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Company Jobs - AstraZeneca Pharmaceuticals



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Kathy @ AstraZeneca Pharmaceuticals

   


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Medical Affairs Leader - Oncology

Gaithersburg MD

Minimum Requirements - Education and Experience Experience, Functional Knowledge, Business Knowledge, Education, Specialist Skills * Relevant advanced scientific or medical degree of appropriate certification (MD Required) * Practical/ working knowledge of the Brand and Disease Area - Oncologya * demonstrated experience with developing medical strategies and plans * demonstrated Experience with global opinion leader engagement Skills and Capabilities * Patient-centred but commercially aware, values driven approach * Level 3/ 4 leadership capabilities * Strong project management skills and extensive experience of managing priority brands * Proven ability to engage, influence and build effective relationships with OLs, across functional and geographic boundaries * Strong verbal and written communication skills in English * Broad understanding of more than one part of the business i.e. Discovery, Clinical, Regulatory, Medical or Commercial roles * Presentation and influencing/negotiation skills (essential) * High ethical standards required

Posted On - 9/22/2014 7:23:31 AM

Sr. Technical Director

Wilmington DE

Minimum Requirements --Education and Experience Functional & Business knowledge Experience, Functional Knowledge, Business Knowledge, Education, Specialist Skills * Have an understanding of the overall drug development and commercialization process from development, launch and through life cycle management * Likely to be educated to PhD level (>10 years relevant experience) or BSc (with >15 years relevant experience), in an appropriate discipline such as Pharmaceutics, Chemical Engineering or other life sciences disciplines and have professional credibility within the business and industry. * Have understanding in the disciplines in Analytical Science, Chemical Science, Formulation Science, Physical/Material Science and global supply chain in order to identify appropriate solutions and deliver value to the organisation. * Have a thorough understanding of principles, applications and management of SHE and cGMP. * Experience in Operations and/or R&D with a track record of successful delivery within a matrix organization. * Evidence of excellent communication skills and build excellent relationships with customers. Skills and Capabilities * Operates confidently as a part of a global organisation, with an integrating mindset, irrespective of function, geographical and company background to help to deliver an organisation prepared for future challenges and change. Demonstrates understanding of change management. * Excellent team working and networking skills and ability to engage relevant AstraZeneca staff * Capable of making effective decisions, acts courageously and communicates with conviction. * An excellent communicator with experience of interacting effectively across interfaces of discipline, culture, and expertise both internally and externally. * Able to demonstrate the drive and energy to establish the role and make a difference. * Demonstrate a high degree of personal credibility. Behaviours: * Focus on delivery under pressure * Lead change effectively * Influencing skills to enable effective management of internal stakeholders and external partners * Good communication skills * Networking skills that enable the necessary links to be formed that allows the group to have high business impact. * Work collaboratively across boundaries. * Personal Technical capability development Preferred requirements Strong pharmaceutics background in formulation and manufacture of sterile products including polypeptide products. Experienced in process validation, understanding and using process capability to identify improvement projects and reduce process variability. Proven track record in leading root cause analysis investigations. Good understanding of raw material attributes, materials science characterization tools including data interpretation and analysis. Training or awareness of lean six sigma Working knowledge in the application of Quality by Design and implementation of new technologies for pharmaceutical testing and manufacture. Good understanding of statistical tools and experience of their application.

Posted On - 9/22/2014 7:23:31 AM

Technician I, Manufacturing

West Chester OH

REQUIREMENTS: Physical Demands Ability to lift 40 pounds, stand for long periods of time, work gowned up for long periods of time, maintain good personal hygiene. Manual Dexterity Unimpaired manual dexterity Audible/Visual Demands Correctable vision equal to or better than 20/20. Environment Manufacturing - Works under conditions with minor hazards such as working with moving machinery and equipment.

Posted On - 9/22/2014 7:23:31 AM

In Vitro ADME Specialist

Cambridge Cambridgeshire

The role will be based in Cambridge The role requires being recognised in a relevant scientific area, and to lead this from the laboratory, making significant contributions to the practical delivery of project goals, whilst working collaboratively with DMPK colleagues locally as well as globally. - Directly impacts the discovery and development portfolio of iMed via specialist guidance and value adding experimental activities. - Is responsible for design, conduct, interpretation and reporting of in vitro ADME studies, working closely with projects. - Provides internally recognised disciplinary scientific leadership, mentors and provide laboratory supervision of less experienced scientists, training and development of scientific talents. This will include personal laboratory work and direct supervision of laboratory science and scientists. - Provides externally recognised disciplinary scientific leadership by leading collaborations with key academic centres and by regularly presenting work through lectures, publications, and reviews in internationally recognized, high impact peer-review journals which raises the scientific reputation of AZ and attracts top scientific talent. - Leads the development and implementation of DMPK scientific strategies and may participate in development of other IMed and/or our late stage Global Medicine Development unit strategies and acts as a catalyst for scientific debate within the AstraZeneca science community. - Identifies leading improvements in technologies that can be successfully applied to a highly competitive drug discovery or development paradigm that contributes to achievement of short and long term business goals. - Provides expert support for due diligence teams as required. - Provides expert peer review of high-level documents, project milestone transitions and in submission development and defence in collaboration with colleagues. Essential Criteria - PhD and post-doc experience or equivalent experience in an ADME related discipline within Pharma Industry and will have made significant contributions to the success of a number of discovery and /or development programs - Significant experience (with a track record of innovation) of a specific DMPK in vitro scientific discipline. Application of this within either discovery or development projects. - Strong publication track record in DMPK in both peer review journals and via oral presentation. - Ability to access science via external collaborations to deliver innovative solutions and significant value to drug discovery and development programs. - Experience in leading small scientific teams containing colleagues to ensure delivery of DMPK in vitro technology/science. Understanding and track record in the application of enzyme/transporter kinetics. - Familiarity with and the application thereof of appropriate regulatory principles and guidelines. Preferred experience/requirements - Experience and the application of Bioanalytical techniques, e.g. LC-MSMS- - Application of both metabolic and transporter science for drug disposition and drug-drug interactions in discovery and development project context. - Application of mathematical modelling techniques within either project setting or in the development of new technology. - Application of Pharmacogenetics to provide understanding to specific DMPK project questions and towards DMPK scientific strategies. - Experience of supervising and mentoring others to ensure delivery of in vitro DMPK technologies, to address specific DMPK project issues or to provide improvements to core technologies. Other - Strong oral and written communication skills - Strong collaborative skills For more information about the position please contact: Katherine Fenner on +44 (0) 7920 845141 Applications close 22nd October 2014.

Posted On - 9/22/2014 7:23:31 AM

IT Service Manager (Collaboration Service Manager)

Macclesfield Cheshire

Service and Supplier Management - Accountable for the delivery of contracted IT services with internal and/or external suppliers and for work with Portfolio Managers to ensure the allocation of service management resources is in line with project and programme portfolio - Owner for effective implementation of service delivery processes, including Incident, Problem, Change, Service Level Management, Financial Management, Capacity Management, Availability Management and Continuity Management for respective service area. - Manage and approve all service changes, improvements and escalations, ensuring that impact on business critical functions is minimised and that the service catalogue is up-to-date - Ensure collaboration with other service managers and capability leads on communication of Service Improvement Plans and provide input into assessment of customer satisfaction & improvement plans - Deliver maximum operational value to AZ from relationships with internal and external suppliers, serving as the main contractual lead representing AZ to external supplier organizations. Service & Financial Performance - Manage internal stakeholder requirements and challenge their thinking so that a solution is developed and delivered that meets expectations in terms of cost and quality. - Drive improvements in service performance ensuring suppliers- performance against SLAs is analysed and used as a benchmark for future SLAs. - Drive the analysis of trends from multiple data sources to inform future improvements. Governance & Tools - Coordinate Service Review Boards and ensuring that customer satisfaction scorecard activities are effectively managed - Develop and maintain the alignment between Supplier Contract Management and Supplier Performance Management, ensuring all process handoffs work correctly. - Ensure effective service management tools, monitoring and processes are implemented in accordance with AZ standards and procedures and to support service management for respective area of responsibility Skills and Experience Essential - Strong experience of developing and managing relationships with both customers and suppliers - ITIL V3 Practitioner or fully operational and experience across all aspects of the ITIL service management disciplines and lifecycle within their domain of expertise - Strong communication, facilitation and relationship building skills plus influencing and negotiating skills - Excellent knowledge and experience of risk management and assessment - Communications skills to stakeholders at a senior IT leadership level and proven escalation management capability - Technical expertise for the respective area of the Collaboration expertise in which they are responsible (Messaging, Mobility, Conferencing etc--..) - Industry awareness of latest trends and activity for their respective area of Collaboration Desirable - Business Administration / Information Service Degree - Fully operational and experience across all aspects of the ITIL service management disciplines and lifecycle within their domain of expertise - Ability to work well in diverse, multinational teams and proven ability to influence others to achieve positive outcomes - Financial acumen and experience for running an end-to-end IT service such as Messaging, Mobility, Conferencing.. etc.... - Experience of running developments and improvements to a globally consumed service with multiple demand channels. Additional Information The closing date for this role is midnight 20th October 2014. We offer a competitive salary. You can apply via www.astrazeneca.com/careers using the reference number IT14290-1 in the keyword search

Posted On - 9/22/2014 7:23:31 AM

Reporting and Big data Capability Lead

Luton Bedfordshire

The International IT Reporting and big data Capability Lead will also build and retain the platform expertise for the Region and secure effective services remain after implementations. - Lead coordination of Global Commercial Reporting and big data platform delivery across Markets - Ensure Fit of Global solutions versus Business mandatory requirements and Market local constraints, and proper integration with remaining legacy systems - Drive local systems decommissioning linked to the Global platform delivery, Govern the platform implementation and local move to Cloud Business Information platform. - Drive change linked to Global platform delivery through effective governance process on gaps identified in Markets - Leverage platform knowledge and expertise across International through domain reference groups and regular best practice sharing sessions, creating and maintaining a strong community and network of IT personnel - Relevant technical degree or equivalent - Similar experience on Business Information large scale Strategy definition and implementation - Demonstrated ability in the successful delivery of tangible outcomes with significant business value, i.e. they will be practical and delivery-focused as well as strategic, able to create visions and ensure that the vision is delivered - Substantial experience in managing/ delivering IT services including the initiation, scoping and delivery of major projects - Proven skills and experience managing and controlling large project and programme budgets - Demonstrated ability to influence and build strategic working relationships with senior AZ internal customers, peers and vendors - specific understanding and experience of sales and marketing activities highly desirable. - Experience working in a global organization where stakeholders and project team members are geographically dispersed. - Proven experience of leading change, using different approaches and methodologies - Proven ability to interpret/ communicate technical information into business language - Managing, developing and leading a team of people in different locations - Internally as well as externally focused with multicultural awareness and flexibility to operate across functions and hierarchies - Awareness of developments in the marketplace and understand the relevance and potential impact to AZ IT · Excellent communicator in written and oral English · · In addition, candidates will be expected to demonstrate: · Significant project delivery and Business Analysis experience · Influencing and Innovation skills · Good communication skills and facilitation skills with the ability to work with others to achieve objectives..

Posted On - 9/22/2014 7:23:31 AM

Programming Team Leader

Cambridge Cambridgeshire

Function / Team R&D -> GMD -> Biometrics & Information Sciences -> Programming * B&I drives good design to generate the data needed for quality decision making. The goal of B&I is to deliver value to the pipeline by excellence in delivery, improving decision making, and engaging and shaping the external environment whilst accessing and implementing innovative solutions. * Programming is the department that oversees and delivers the programming aspects of clinical development , manages and maintains the end to end standards and manages and maintains the Analysis and Reporting production tools and the information infrastructure. * Therapeutic Area Programming is the group that oversees and delivers all the programming contribution to internal decision making, regulatory submissions and reporting and commercial activities for the Therapeutic Area portfolio of projects. Candidate Focus & Challenge - Therapeutic Area (TA) level accountability for quality and standards of study/project programming deliverables, including holding partners and providers accountable for their contributions - Strategic focus - understanding drug development to support the full project lifecycle - Leading programming contributions within and across Projects for a TA and including data integration strategies, regulatory submissions, and timely responses to regulatory questions - Building and managing relationships to create the conditions for success for our global project teams - Thriving in a dynamic, fast-paced environment, with a strong emphasis on collaboration and working across functional/geographic boundaries - Leveraging tools beyond SAS to transform of data into information and facilitate improved decision making (e.g., S-Plus, R, visual analytics, BI tools) - Contribute to the development of best practice to improve quality, efficiency and effectiveness - Line manage a team of Principal and Senior Programmers for the projects they lead Candidate Knowledge, Skills & Experience, must have: - BSc (or local equivalent) in Mathematics, Statistics, Informatics, Life or Social Sciences - Extensive statistical programming or other relevant functional-area experience in a Phase III environment, to an expert level - Very strong leadership profile, excellent communication and problem-solving skills - Advanced project management and stakeholder management abilities - Expert knowledge of CDISC standards (CDASH, SDTM, ADaM) and their application - Comprehensive knowledge of GCP and applicable technical/regulatory requirements - Demonstrated experience with regulatory submissions - Experience managing external vendors and working with industry partners Opportunities to Grow with AstraZeneca -Play a role in delivering our new vision for Programming -Drive ongoing development of therapeutic area data and reporting standards -Coach and mentor colleagues to success -Be part of building our new analysis and reporting environment -Represent Programming at external conference and forums -Work with outstanding professionals focused on science, quality, and helping patients AstraZeneca Making a Difference AstraZeneca is an equal opportunity employer Please note that this role offers a competitive salary and will close on 30th September 2014 and can be based in Cambridge UK, Sweden or US

Posted On - 9/22/2014 7:23:31 AM

IT Solutions Delivery Lead

Cambridge Cambridgeshire

This will be achieved by: · Establishing working relationships with the IMED and GMD customer group to develop an understanding of business priorities and insight into changing needs in order to inform and shape demand. · Contribute to the development and delivery of IS portfolio of services and projects aligned with the drug development business and strategies. · Contribute to the efforts to understand the business needs and analyse, validate and document the business and system requirements that address these needs. · Use knowledge and understanding of the IMED and/or GMD business area direction and priorities to drive innovative solutions to issues and challenges faced by the customer area. · Contribute in developing the capabilities (methods, processes, best practices etc.) in at least one of the Programme- Project- Service Management, Business Analysis or Business Relationship Management capabilities. · Delivery of excellent services to the IMED and GMD business units, and support service management activities to ensure that services are delivered in accordance with Service Level Agreements and business requirements. · Support less experienced Project/Service Managers and/or Business Analysts in the execution of their duties. Successful candidates will be required to demonstrate the following capabilities & skills: · Bachelors degree in Computer Science with strong experience in software solutions delivery · Degree or experience in life sciences/pharmaceuticals industry is an asset · A strong understanding of the processes, stages, activities, and major decision points in preclinical or clinical drug development. · Understands the interdependencies between the deliverables of the key business functions in pharmaceutical R&D · Ability to apply this knowledge to solve problems and knows when to enlist help from others. · Established knowledge of or some experience of working in a specific disease or therapy areas. · Established knowledge of scientific domain, e.g. some experience in working in the scientific domain. · A good understanding of the scientific theory of the scientific domain · A good understanding of the techniques and approaches applied in the scientific area of expertise and how to interpret to derive useful information. · Competency coping with standard problems/common situations, competent at day-to-day application of the capability, and is able to apply and present concepts, information and solutions. We offer a competitive salary for this role The role will close at midnight 2nd October 2014 To apply please visit www.astrazeneca.com/careers and use the keyword ITRRDI03

Posted On - 9/22/2014 7:23:31 AM

Brand Manager -- HCP (Gout Franchise)

Gaithersburg MD

Minimum Requirements: * Bachelor's Degree; preferably in a relevant field * 5 years of pharmaceutical or healthcare; preferably related experience * 5 + years marketing; preferably Promotions experience and/or Sales experience * Experience in Project Management Preferred Background: * MBA in relevant field * Experience working with a collaboration/external partner * Experience in Consumer, Managed Markets, Insights roles * Experience in customer-facing roles * Exceptional interpersonal, communication, leadership, and facilitation skills

Posted On - 9/19/2014 7:11:19 AM

Product Manager

Wilmington DE

Education, Qualifications, Skills and Experience Essential * Bachelor's degree in science/healthcare related field or proven Patient Safety experience equivalence in a similar role, and an excellent clinical background. In exceptional circumstances 10-15 years of drug safety experience will be considered in lieu of degree requirement * At least 3 years patient safety experience * Demonstrated working knowledge of FDA and ICH regulations relevant to Patient Safety and adverse event reporting Desirable * Advanced degree in science/healthcare-related field * 3-5 years drug safety experience * At least 2 years clinical practice experience * Working knowledge of surveillance of pharmaceutical products * Working knowledge of epidemiology and/or clinical research experience * Demonstrated capabilities in: Project management, Time management, Presentation skills, Strong attention to detail and organization

Posted On - 9/19/2014 7:11:19 AM

Team Leader

Wilmington DE

Education, Qualifications, Skills and Experience Essential * Bachelor's degree in science/healthcare related field plus proven Patient Safety surveillance experience equivalence, and an excellent clinical background. * At least five years patient safety experience and/or at least five years clinical or pharmaceutical experience * Demonstrated working knowledge of FDA and ICH regulations relevant to Patient Safety and adverse Desirable * Advanced degree in science/healthcare-related field * Ability to synthesize and analyze complex medical and scientific data * Working knowledge of epidemiology * Demonstrated capabilities in: Project management, Time management, Presentation

Posted On - 9/19/2014 7:11:19 AM

Patient Safety Special Relationship Scientist

Gaithersburg MD

Minimum Requirements: * Qualified to degree level in biosciences or an equivalent healthcare or pharmaceutical industry background with proven competence in Patient Safety/Clinical Development * The ability to travel both domestically and internationally * Proven project management skills and experience managing and controlling large projects /programs * Demonstrated understanding of quality and compliance * Excellent communication, relationship management, and influencing skills * Proven track record negotiating across complex groups * Experience working in global organization and across cultural boundaries where stakeholders and project team members are geographically dispersed * Strong knowledge and experience with Patient Safety or Regulatory systems (Life Science - pharmaceutical software) * Evidence of shaping innovative solutions that have a major impact within the business area and organization * Excellent business acumen with sensitivity to environment * Self-starter, motivated and positive with ability to work with a high degree of autonomy in a dynamic environment. * Long term vision -- strategic thinker. * Able to represent AstraZeneca externally where required * Maintains high ethical standards, including a commitment to AstraZeneca values and behaviors Preferred Background: * 3-5 years Alliance management, and 5-7 years Global Regulatory, Patient Safety and/or Clinical Development experience * MBA * Experience leading inspections/inspection activities * Excellent knowledge of Regulatory Environment (e.g. FDA, MHRA, EMEA, other key markets/areas) * Change management experience

Posted On - 9/19/2014 7:11:19 AM

Global Regulatory Intelligence Director

Cambridge Cambridgeshire

Queries & Regulatory Strategy Documents (RSDs) * Work collobaratively to effectively respond to queries in support of robust RSD creation * Leads/oversee delivery of regulatory environment components of RSDs: * using knowledge of broad regulatory issues with emphasis on cross-cutting matters * leveraging institutional memory, and disease area specific investigations * Review of assessment reports published by key regulatory authorities (e.g., EMA EPARs; US FDA's SBAs; etc.,) and output from relevant meetings (e.g. US FDA Advisory Committees) and ensure RSDs and environment documents reflect this intelligence Metrics * Endorse/ implement change based on metrics. * Coordinate collection and use of internal and externally gathered metrics * Communicate results of analysis to broader business, and use to shape external environment. Account Manager * Manage relationships with external vendors such as CIRS, CMR, Tufts, etc * Drive development of business case in order to acquire further services from suppliers which require additional budget * Within budget, optimize delivery of services from vendor and identify if further services are required Internal Engagement * Create and Manage overall internal engagement strategy. * Build internal networks on complex regulatory topics. * Manage relationship with senior management, e.g., legal, TAVPs, etc. * Establish & leverage relationship with specific accounts (other AZ functions, policy and CI groups, etc) as assigned. * Identify gaps, analyze business requirements and implement improvements. * Represents AZ on internal issue based teams. External Engagement * Represents and advocates on behalf of AZ on broader regulatory and drug development intelligence topics * Represent company on external network for multiple and cross-functional topics and/brief senior management in advance of key meetings. * Endorse, prioritize external engagement and monitoring topics. * Provide a broad strategic view for regulatory intelligence issues that form the basis of GRAPSQA's external engagement activities * Chair multiple topic external networks/committees, as appropriate * Develop networks with external senior RA staff * Provide timely, constructive feedback and coaching to direct reports and AZ colleagues Minimum Requirements --Education and Experience * Advanced degree in a scientific/public policy/legal field * Demonstrated expertise within US and/or EU and/or/International Health Authorities involved with both product and intelligence related matters. * Working knowledge of AZ focused disease areas. * Understanding of how drugs are commercialized in the US and/or EU/International markets. * Excellent leadership, collaboration and influencing skills, with proven ability in x-functional projects. * Excellent written and verbal communication skills. * Thorough scientific knowledge sufficient to understand all aspects of regulatory issues. Internal and External Contacts/Customers * GRAPSQA US, EU, and International Leadership team * AZ senior leadership teams, i.e., SET, GDD/SMT, TAs, etc. * Policy and Intelligence colleagues GRAPSQA Regional VPs * GPTs, Other SET Functions and teams as required by issues. * Other Leadership teams, i.e., Government Affairs, Corporate External Relations, Legal, Promotional Regulatory Affairs (PRA), etc. * Key External Regulatory opinion leaders * US, EU/International Trade Organizations, Professional Associates, and related global regulatory networks * External system suppliers Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation

Posted On - 9/19/2014 7:11:19 AM

Device Technical Director

Alderley Park Cheshire

Minimum Requirements - Education and Experience * This role has been created to support our ambitious Inhalation Strategy ? so Inhalation device experience is desirable not critical * Have an understanding of the overall drug and device development and commercialization process from development, launch and through life cycle management * Significant experience of working with devices as a device design engineer or device quality engineer working in product development and/or operations * Likely to be educated to PhD level or BSc with experience in an appropriate discipline and have professional credibility within the business and industry * Have understanding in the disciplines in Packaging and Device development, analytical, formulation and physical Science and global supply chain in order to identify appropriate solutions for management of devices and deliver value to the organisation * Have a thorough understanding of principles, applications and management of SHE, cGMP and medication device/combination product standards and legislation * Experience in Operations and/or R&D with a track record of successful delivery within a matrix organization * Evidence of excellent communication skills and building excellent relationships with customers. Skills & Capabilities * Operates confidently as a part of a global organisation, with an integrating mindset, irrespective of function, geographical and company background to help to deliver an organisation prepared for future challenges and change. Demonstrates understanding of change management * Excellent team working and networking skills and ability to engage relevant AstraZeneca staff * Capable of making effective decisions, acting courageously and communicating with conviction * An excellent communicator with experience of interacting effectively across interfaces of discipline, culture, and expertise both internally and externally * Able to demonstrate the drive and energy to establish the role and make a difference * Demonstrate a high degree of personal credibility * Focus on delivery under pressure * Lead change effectively * Influencing skills to enable effective management of internal stakeholders and external partners * Good communication skills * Networking skills that enable the necessary links to be formed that allows the group to have high business impact * Work collaboratively across boundaries * Personal Technical capability development

Posted On - 9/19/2014 7:11:19 AM

Device Technical Manager

Alderley Park Cheshire

Minimum Requirements - Education and Experience * This role has been created to support our ambitious Inhalation Strategy ? so Inhalation device experience is desirable not critical * Have an understanding of the overall drug and device development and commercialization process from development, launch and through life cycle management * Significant experience of working with devices as a device design engineer or device quality engineer working in product development and/or operations * Likely to be educated to PhD level or BSc with experience in an appropriate discipline and have professional credibility within the business and industry * Have understanding in the disciplines in Packaging and Device development, analytical, formulation and physical Science and global supply chain in order to identify appropriate solutions for management of devices and deliver value to the organisation * Have a thorough understanding of principles, applications and management of SHE, cGMP and medication device/combination product standards and legislation * Experience in Operations and/or R&D with a track record of successful delivery within a matrix organization * Evidence of excellent communication skills and building excellent relationships with customers. Skills & Capabilities * Operates confidently as a part of a global organisation, with an integrating mindset, irrespective of function, geographical and company background to help to deliver an organisation prepared for future challenges and change. Demonstrates understanding of change management * Excellent team working and networking skills and ability to engage relevant AstraZeneca staff * Capable of making effective decisions, acting courageously and communicating with conviction * An excellent communicator with experience of interacting effectively across interfaces of discipline, culture, and expertise both internally and externally * Able to demonstrate the drive and energy to establish the role and make a difference * Demonstrate a high degree of personal credibility

Posted On - 9/19/2014 7:11:19 AM

Sr. Director Physician, Early Clinical Development - Oncology

Cambridge Cambridgeshire

Education, Qualifications, Skills and Experience Essential: * Graduate of a recognized school of medicine with an M.D. degree or equivalent * >5 years clinical research expertise in oncology, in designing, monitoring and implementing clinical trials and interpreting trial results * Specialty training or board eligibility in hematology/oncology * Significant leadership experience * >5 years Drug Development Experience with a thorough understanding of pharmaceutical safety, reporting and surveillance processes * At least 5 years early clinical translational research expertise and experience, including experience in designing, monitoring, executing and interpreting clinical trials, with understanding of biomarkers, biostatistics and safety reporting * Proven teamwork and collaboration skills * Technical (medical and scientific) experience evaluating targets/agents for in -licensing or internal development * Ability to travel nationally and internationally * Organize and deliver Advisory Boards with international KOLs * A clear demonstration of behaviours of o Truth seeking rather than success seeking o Agile responsiveness to scientific data o Embracing of peer review o Agnostic to internal-external sourcing Preferred : *PhD in scientific discipline * Extensive general medical knowledge * Experience in several organizations and geographic locations Key Relationships to reach solutions Internal (to AZ or team) External (to AZ) Senior management team Global business leaders Regulatory and Finance colleagues Transaction and deal specialist colleagues Strong external awareness, good international scientific and external decision-maker-networks Credibility in scientific, regulatory and commercial environments Academic partners, partners in cross-company initiatives, CROs, Public Private Partnership consortia Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation

Posted On - 9/18/2014 8:05:50 AM

Pharmaceutical Sales Specialist - PC - Hollywood, FL

Hollywood FL

Qualifications: Education: -Bachelors degree (any major) from an accredited college or university is required. Experience: - Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required - Demonstrated effective organizational and communication skills - Leadership, self--motivation and initiative - Demonstrated judgment and decision-making capability - Be results oriented with demonstrated time management skills - Ability to learn, analyze, understand and convey complex information - Demonstrated technical aptitude and computer skills are essential - A valid driver's license and safe driving record

Posted On - 9/18/2014 8:05:49 AM

Scientist, Technical Operations

West Chester OH

QUALIFICATIONS Education: Bachelors degree in Chemistry or Pharmaceutical Sciences, advanced degree preferred. Experience/Skills: Strong background (7-10+ years of experience) with a wide range of analytical characterization techniques and equipment. Proficient in statistical analysis. Experience in leading and working on diverse cross-functional teams. GMP experience required.

Posted On - 9/18/2014 8:05:49 AM

QCI / Sr. QCI Manager (Brand Insights)

Wilmington DE

QCI Manager Advanced Quantitative degree in one of the following fields: Economics, Operations Research, Statistics, or Engineering 2+ years of experience in ANOVA-ANCOVA, Regression Analysis, Optimization and Simulation (with an emphasis on probability and statistics) 2+ years of experience with SAS/Base, SAS/Stat, Excel, Word, and PowerPoint 1+ years of experience in designing & executing analyses, as well as delivering insights, related to one or more of the following: Response analytics; marketing mix optimization; size, structure & resource allocation across diverse personal promotional channels; promotional targeting (both personal and non-personal); 1+ years of Project Management experience Sr. QCI Manager Advanced Quantitative degree in one of the following fields: Economics, Operations Research, Statistics, or Engineering 4+ years of experience in ANOVA-ANCOVA, Regression Analysis, Optimization and Simulation (with an emphasis on probability and statistics) 4+ years of experience with SAS/Base, SAS/Stat, Excel, Word, and PowerPoint 1+ years of experience in designing & executing analyses, as well as delivering insights, related to one or more of the following: Response analytics; marketing mix optimization; size, structure & resource allocation across diverse personal promotional channels; promotional targeting (both personal and non-personal); 1+ years of Project Management experience Preferred Requirements: Ability to work collaboratively with and influence peers and management. Ability to think strategically. Strong verbal and written communication skills.

Posted On - 9/17/2014 7:31:40 AM

Wireless Engineer- UK

Cambridge Cambridgeshire

Skills & Capabilities Essential - Experience in designing and configuring Cisco routers and switches - Experience in Design and implementation in LAN Technologies. - Experience working with Cisco Nexus Servers. - Experience working with TACACS. - Experience implementing and administering QOS. - Knowledge and Experience working within a Service Oriented Engineerure. - Ability to document and maintain Network support documentation (e.g., processes procedures, workflows, communication/training material, service catalog, etc.) - Ability to support the integration and organizational adoption of IT processes, standards, policies and controls - Strong relationship management experience - Excellent communication skills, both written and verbal, and excellent presentation skills. - Experience with SNMP configuration, tooling and log correlation leveraging syslog and regular expressions and common log collection tools such as SPLUNK - Proficient with common Netflow tools, such as NetQoS and OpNet - Proficient with common Wireless network tools such as AirMagnet, AirWave, and NCS Prime Infrastructure. - Advanced features (Netflow, IPSLA, NBAR) - Familiar with LAN & WLAN technologies - Must be able to execute end to end processes based on ITIL framework - Must have experience of working in a multi partner scenario and a cross- culture environment. Desirable - A minimum of a Bachelor's Degree is required, MS or MBA preferred. - Sound knowledge of Release Management, Incident Management and Problem Management processes. - Experience working in globally distributed team Ability to work as part of a team through challenges faced in highly customized environments.

Posted On - 9/17/2014 7:31:40 AM

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