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| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Director, Research, Development and Global Compliance |
| 1. Bachelors of Science degree in a health science related field required. PharmD or Advanced degree preferred. 2. 5 -10 years pharmaceutical industry experience required with at least 5 years in a research & development functional area. Scientific/Medical Liaison experience a significant plus. 3. Prior pharmaceutical compliance department experience and/or demonstrated knowledge of industry compliance issues.4. Prior experience managing one or more direct reports preferred. 5. Demonstrated leadership skills and strategic focus. Demonstrated ability to exercise independent judgment and effectively collaborate with multiple functional units. 6. Excellent oral and written communication, presentation, teaching and coaching skills.7. Demonstrated ability to manage multiple projects simultaneously with little or no supervision. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Associate Medical Director/Medical Director, Medical Affairs, |
| M.D. degree, Board Certified or Board Eligible in Designated Specialty (preferred) with subject matter expertise in dermatology or ImmunologyThree years clinical or clinical research experience preferredOne year experience in the pharmaceutical industry preferredExcellent communication and presentation skills, strong interpersonal skills.Strong clinical research/medical affairs background, and excellent problem solving abilities.Demonstrate abilities to work effectively in a team environment.Ability to interpret and evaluate clinical data. Leadership skills and ability to effectively manage projects and timelines. Knowledge of pharmaceutical clinical development and ability to effectively apply technical principles, theories, and concepts to clinical drug development. Knowledge of FDA, other regulatory agency and professional requirements, regulations and guidancesAble to work independently on all aspects of assigned projectsExcellent organizational skills |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate Antibody Production, Agensys - Santa Monica, CA |
| ?X Bachelors, or Masters Degree in Cellular Biology, Bioengineering, Microbiology or a related field. ?X Minimum of 2 years post graduate experience. ?X Extensive mammalian tissue culture experience, preferably gained in an antibody production environment. ?X Knowledge of process development for antibody production from hybridomas or recombinant cells; experience with techniques to improve recombinant protein expression by stable mammalian cell lines is advantageous?X Applicants should be well organized, self-motivated, and capable of working independently and in a collaborative environment. ?X Experience in antibody purification techniques is desirable but not essential as full training will be given.?X Excellent verbal and written communication?X Excellent organizational skills. ?X Meticulous note keeping will be essential |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate, Cell Line Development - Agensys, Santa Monica, CA |
| The ideal candidate will have a M.S. or B.S. in Molecular Biology or related field, with preferably a minimum of three (3) years of relevant experience in industry. Experience in antibody expression systems, production cell line generation, and antibody characterization is required. Excellent verbal and communication skills, as well as the ability to work in a team environment are essential. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Research Fellow |
| Education:Ph.D. degree in biochemistry, pharmaceutical sciences or a related field Required:A broad understanding of the pharmacokinetics and disposition of therapeutic proteins. 3 or more years of industrial or academic experience in DMPK support of Biologics discovery/development programs. Excellent written and verbal communication skills. Preferred:Three or more years of industrial or academic experience in pharmacokinetic/pharmacodynamic (PK/PD) modeling. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #PHA000871. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
 AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Director Field Medical Physician (CV) |
· Graduate of a recognized medical school and recipient of an M.D. degree
· Range of 11 - 33 years of clinical practice
· Board certification in cardiology
· Background in academic medicine, clinical research, and familiarity with biostatistics
· Excellent written and oral communication, interpersonal, and organization skills
· Demonstrated ability to proactively and positively engage teams through multiple communications channels including telephone, e-mail, Internet, and face-to-face
· Ability to travel nationally and internationally
Preferred Background
· Other training such as an M.P.H. or other advanced degree
· Experience with or business acumen around working within the pharmaceutical industry
· Experience with pharmaceutical drug development and medical/scientific affairs
· National recognition as a key opinion leader as demonstrated by a track record of scholarship, independent research funding, publications, and membership in national societies
· Familiarity with DDMAC, PhRMA code, and key regulations in the pharmaceutical industry
· Geographically located close to Wilmington, Delaware headquarters
 |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Sr Safety Assessment Expert |
| PhD in pharmacology, toxicology or a related biological science; MD with appropriate experience, DVM with appropriate training and experience. PharmD or equivalent with a strong biological background or equivalent work experience.
Languages: Fluent English (oral and written).
Experience/Professional requirement:
1. Level-dependent.
o Base level: At least 2 years experience as a part-time safety assessment project team representative alongside other duties such as study director; experience with biologicals safety assessment desirable.
o Senior level: At least 3 years experience as a full time safety assessment project team representative, preferably with a mix of research, exploratory development and full development teams including experience of biological products
o Principal level: At least 5 years experience as a senior level safety assessment PTR and internal recognition as an opinion leader in one or more aspects of safety assessment, or the equivalent experience in a similar external organization. Experience of biologics safety assessment required.
2. Advanced knowledge of the many scientific disciplines involved in biopharmaceutical drug safety assessment and the relevant laboratory tools and procedures related to safety assessment and risk management, including PK-PD aspects of study design and data interpretation
3. Documented expertise in scientific and technical problem-solving in an international, multi-disciplinary, project-driven environment.
4. Proficient with full range of techniques used in job and core area?especially with communication and negotiation with global health authorities.
5. Detailed knowledge of drug development processes and worldwide regulatory guidelines and procedures.
6. Ability to manage conflicting expectations in a matrix environment.
7. Proven negotiation skills.
8. Excellent program and project management skills.
9. Team player behavioural attributes.
10. Self-motivated and able to operate independently.
11. Ability to coach and advise colleagues in project-related matters (at senior and principal levels). |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Onco Dir Clinical Rsch Phys |
| ? MD or PhD in Clinical Parmacology, Biochemistry or related field
? Substantial postgraduate bedside or clinical pharmacology experience in a relevant cancer treating discipline and institution required.
? Substantial experience with determining, administering, and evaluating the outcome of systemic combined modality cancer or adult hematologic malignancy treatment plans required.
? ? 3 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV.
? Medical/scientific and operational expertise in cancer molecular medicine, biologics, and or response modifiers
? Demonstrated technical knowledge and innovation in early clinical development study designs that provide relevant evidence to decision-makers.
? Versatile knowledge and understand of pre-clinical science of oncology and all aspects of translational medicine such as toxicology, pharmacology, and regulatory requirements for early phase development in at least two relevant jurisdictions |
| Merck & Co., Inc. |
Upper Gwynedd |
PA |
11/19/2009
|
| Director Clinical Research, Oncology |
| · M.D or M.D./Ph.D who is Board Certified or Eligible in Oncology (and Hematology);· Must have experience in industry or academia;· Demonstrated record of scientific scholarship and achievement;· A proven track record in clinical medicine and background in biomedical research is essential;· Prior specific experience in clinical research and prior publication is desirable but not necessary; and· Strong interpersonal skills, as well as the ability to function in a team environment are essential. About MerckConsistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world.We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation.To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CLI001839. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.Our work is someone's hope. Join us.Where patients come first - MerckSearch Firm RepresentativesPlease Read Carefully:Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Agilent Technologies, Inc. US |
|
MA |
11/20/2009
|
| Account Manager-Life Science Research |
| - BS/BA Degree or equivalent in molecular biology or equivalent
- 1+ years research experience
- 3+ years related direct life science product sales experience with a demonstrated track record of successfully selling against a quota.
- Demonstrated business development and sales closing skills.
- Good written and verbal communication skills.
- Ability work within a team selling environment.
- Ability to interface with all levels within an organization for both internal/external customers.
- Experience with pharmaceutical, biotech and academic customers a plus.
Geo Location: Cambridge, MA
~cb~09/09/09 |
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