Charlottesville
VA
Four year college degree required or its international equivalent or related experience
? Financial-related experience preferred
? Demonstrated proficiency of MS Excel (testing)
? Experience using information systems and MS Office (MS Word/Excel/PowerPoint) preferred
? Experience within the CRO Industry required
Posted On -
5/22/2013 5:58:00 AM
Lenexa
KS
* An undergraduate degree, its international equivalent in health sciences, auditing, etc. from an accredited institution or sufficient previous experience in auditing is required.
* Read, write and speak English; fluent in host country language required.
* 1?2 years experience working the clinical, regulatory, or quality environment within CRO/ pharmaceutical / healthcare environment.
* Excellent verbal and written communication skills, interpersonal skills
* Excellent organizational skills
* Must possess a technical knowledge that is applicable to clinical drug development and posses the expected ability to master the needed understanding of clinical and technical areas.
Posted On -
5/22/2013 5:58:00 AM
Charlottesville
VA
· Undergraduate degree or equivalent experience required. Undergraduate degree in allied health, bio-medical, information systems related field preferred.
· Minimum 5 years experience in clinical research.
· Excellent written and oral communication skills.
· Proficiency in and experience managing the implementation of at least one Clinical Informatics system required.
· Minimum 2 years experience in a lead role.
· Project financial management experience required.
· Experience managing technical vendors for system/data integration.
· Proficient at utilizing systems to provide study and/or data metrics.
· Familiar with clinical development and product life cycle terminology.
· Experience working with data review committees preferred.
· Regulatory submission knowledge and/or experience preferred.
· Managing data deliverables according to CDISC standards preferred.
Posted On -
5/21/2013 5:51:18 AM
Horsham
PA
· Undergraduate degree or equivalent experience required. Undergraduate degree in allied health, bio-medical, information systems related field preferred.
· Minimum 5 years experience in clinical research.
· Excellent written and oral communication skills.
· Proficiency in and experience managing the implementation of at least one Clinical Informatics system required.
· Minimum 2 years experience in a lead role.
· Project financial management experience required.
· Experience managing technical vendors for system/data integration.
· Proficient at utilizing systems to provide study and/or data metrics.
· Familiar with clinical development and product life cycle terminology.
· Experience working with data review committees preferred.
· Regulatory submission knowledge and/or experience preferred.
· Managing data deliverables according to CDISC standards preferred.
Posted On -
5/21/2013 5:51:18 AM
Lenexa
KS
· Undergraduate degree or equivalent experience required. Undergraduate degree in allied health, bio-medical, information systems related field preferred.
· Minimum 5 years experience in clinical research.
· Excellent written and oral communication skills.
· Proficiency in and experience managing the implementation of at least one Clinical Informatics system required.
· Minimum 2 years experience in a lead role.
· Project financial management experience required.
· Experience managing technical vendors for system/data integration.
· Proficient at utilizing systems to provide study and/or data metrics.
· Familiar with clinical development and product life cycle terminology.
· Experience working with data review committees preferred.
· Regulatory submission knowledge and/or experience preferred.
· Managing data deliverables according to CDISC standards preferred.
Posted On -
5/21/2013 5:51:18 AM
Regional - North America
NA
· Undergraduate degree or equivalent experience required. Undergraduate degree in allied health, bio-medical, information systems related field preferred.
· Minimum 5 years experience in clinical research.
· Excellent written and oral communication skills.
· Proficiency in and experience managing the implementation of at least one Clinical Informatics system required.
· Minimum 2 years experience in a lead role.
· Project financial management experience required.
· Experience managing technical vendors for system/data integration.
· Proficient at utilizing systems to provide study and/or data metrics.
· Familiar with clinical development and product life cycle terminology.
· Experience working with data review committees preferred.
· Regulatory submission knowledge and/or experience preferred.
· Managing data deliverables according to CDISC standards preferred.
Posted On -
5/21/2013 5:51:18 AM
San Diego
CA
· Undergraduate degree or equivalent experience required. Undergraduate degree in allied health, bio-medical, information systems related field preferred.
· Minimum 5 years experience in clinical research.
· Excellent written and oral communication skills.
· Proficiency in and experience managing the implementation of at least one Clinical Informatics system required.
· Minimum 2 years experience in a lead role.
· Project financial management experience required.
· Experience managing technical vendors for system/data integration.
· Proficient at utilizing systems to provide study and/or data metrics.
· Familiar with clinical development and product life cycle terminology.
· Experience working with data review committees preferred.
· Regulatory submission knowledge and/or experience preferred.
· Managing data deliverables according to CDISC standards preferred.
Posted On -
5/21/2013 5:51:18 AM
Lenexa
KS
MINIMUM QUALIFICATIONS:
An undergraduate degree or international equivalent from an accredited institution
1. Previous experience using computerized information systems required; experience with PC Windows and word processing
2. Excellent written and oral communication skills, along with ability to present technical issues.
3. Strong understanding of the clinical programming aspects of clinical research.
4. Demonstrated experience applying at least one data standard such as: CDASH, SDTM and ADaM.
5. Strong understanding of the practical implementation of data standards to data management, clinical programming or biostatistics.
6. Read, write and speak English; fluent in host country language required
PREFERRED:
1. Experience developing and maintaining a global library
2. Experience participating in governance of a library of standards
3. Experience of ETL tools (e.g. EXACT) used for the creation of SDTM or ADaM datasets.
4. Experience creating and delivering training materials
Posted On -
5/21/2013 5:51:18 AM
Horsham
PA
(MINIMUM)
* Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution or a licensed health-care professional (i.e., registered nurse) required.
* Read, write, and speak fluent English, fluent in host country language.
* Substantial experience using computerized information systems, Outlook, Word, Excel, PowerPoint, and
* CTMS required.
* Minimum 3 years of clinical research experience required or equivalent regulatory experience.
* Experience in managing and in meeting agreed targets on clinical deliverables during the start-up phase of a project.
* Multi-country coordination experience or exposure to more than 1 country + cross cultural awareness.
* Thorough knowledge of ICH GCP and knowledge of local regulatory authority regulations regarding drug research and development required.
* Thorough knowledge of local clinical start-up process and requirements required.
PRA is an Equal Employment Opportunity / Affirmative Action Employer
Posted On -
5/20/2013 6:10:39 AM
Raleigh
NC
(MINIMUM)
* Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution or a licensed health-care professional (i.e., registered nurse) required.
* Read, write, and speak fluent English, fluent in host country language.
* Substantial experience using computerized information systems, Outlook, Word, Excel, PowerPoint, and
* CTMS required.
* Minimum 3 years of clinical research experience required or equivalent regulatory experience.
* Experience in managing and in meeting agreed targets on clinical deliverables during the start-up phase of a project.
* Multi-country coordination experience or exposure to more than 1 country + cross cultural awareness.
* Thorough knowledge of ICH GCP and knowledge of local regulatory authority regulations regarding drug research and development required.
* Thorough knowledge of local clinical start-up process and requirements required.
PRA is an Equal Employment Opportunity / Affirmative Action Employer
Posted On -
5/20/2013 6:10:39 AM
Regional - North America
NA
(MINIMUM)
* Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required.
* Read, write and speak fluent English; fluent in host country language
* 5+ years of clinical research experience required, including at least 2 years experience in clinical trial management
* Must have strong experience with Respiratory or Infectious Disease Studies
Posted On -
5/20/2013 6:10:39 AM
Regional - North America
NA
(MINIMUM)
* Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required.
* Read, write and speak fluent English; fluent in host country language
* 5+ years of clinical research experience required, including at least 2 years experience in clinical trial management
* Must have strong experience with Respiratory or Infectious Disease Studies
PRA is an Equal Employment Opportunity / Affirmative Action Employer
Posted On -
5/17/2013 7:19:55 AM
Raleigh
NC
(MINIMUM)
* Undergraduate degree or its international equivalent in clinical, science, or health related field from an accredited institution or a licensed healthcare professional
* Minimum of 2 years of related experience
* Experience with PC-Windows, word processing, and electronic spreadsheets required.
* Knowledge of ICH and local regulatory authority drug research and development regulations required.
* Clinical trials support or pharmaceutical industry experience required.
* PRA is an Equal Employment Opportunity / Affirmative Action Employer
Posted On -
5/17/2013 7:19:55 AM
Charlottesville
VA
· An undergraduate degree or its international equivalent in business, finance or health sciences from an accredited institution, or equivalent work experience
· Proven ability to use all MS Office suite including Word, Excel, Access, Powerpoint
· Basic functional knowledge of MS Project preferred
· Read, write and speak fluent English; fluent in host country language
· Experience in clinical biomedical research preferred
· Familiarity with medical terminology required
Posted On -
5/17/2013 7:19:55 AM
Raleigh
NC
· An undergraduate degree or its international equivalent in business, finance or health sciences from an accredited institution, or equivalent work experience
· Proven ability to use all MS Office suite including Word, Excel, Access, Powerpoint
· Basic functional knowledge of MS Project preferred
· Read, write and speak fluent English; fluent in host country language
· Experience in clinical biomedical research preferred
· Familiarity with medical terminology required
Posted On -
5/17/2013 7:19:55 AM
Lenexa
KS
Requirements:
* A high school diploma and/or equivalent
* Experience with medical terminology
* 1-2 years work experience in related field
* Read, write, and speak English
About Early Development Services
PRA's Early Development Services (EDS) group, is one of the business units within PRA that provides comprehensive services such as Phase I and IIa clinical research, Bioanalytical research and Data support. PRA's facilities are located in the United States, The Netherlands and Central Europe. Over 700 professionals working from different countries make up PRA's Early Development Services team and work together to get the best result.
Part of EDS is a Clinical Pharmacology Center in The Netherlands with 140 beds divided over two separate Clinical Research Units (CRU) located in Groningen and Zuidlaren. In this CRU we do research into the effects and possible side effects of medicines. This is done with the help of volunteers both healthy people and patients. Research on humans is a mandatory step in the development of new drugs before they are marketed. Within the facility we have a GLP-compliant clinical laboratory and a GMP-compliant pharmacy which provides sophisticated compounding.
Posted On -
5/17/2013 7:19:55 AM
Lenexa
KS
QUALIFICATIONS
? Medical degree.
? At least 2 years clinical experience (or 1 year in Phase I unit).
Posted On -
5/17/2013 7:19:55 AM
Raleigh
NC
QUALIFICATIONS
? Medical degree.
? At least 2 years clinical experience (or 1 year in Phase I unit).
Posted On -
5/17/2013 7:19:55 AM
Raleigh
NC
QUALIFICATIONS
? Undergraduate degree in clinical, science, or health-related field from an accredited institution,
or equivalent work experience required
? Advanced degree (e.g., M.S., M.B.A., Pharm.D.) preferred
? Proven skills with industry standard clinical data management systems (Oracle Clinical, Clintrial,
eData Management) or electronic data capture (EDC) software required
? Multifunctional experience with clinical data management activities required
? Experience supervising or managing professional staff required; management experience in the
pharmaceutical, biotechnology or CRO industry is preferred
Posted On -
5/17/2013 7:19:55 AM
Lenexa
KS
* A high school diploma and/or equivalent
* 2 ? 4 Years of related experience.
* Ability to gather, recommend and summarize data for reports, finds solutions to various administrative problems, and prioritizes work.
* Work requires attention to detail in composing, typing and proofing materials, establishing priorities and meeting deadlines.
Posted On -
5/17/2013 7:19:55 AM
|