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Online Resumes with "Drug Accountability"

Featured Profile

Clinical Research Associate

SUMMARY OF QUALIFICATIONS • Foreign graduate Medical Doctor and licensed RN with more than 22 years of clinical and research experience. US citizen. Fluent in English, Russian and Romanian • Extensive training in Good Clinical Practices, ICH Guidelines, SOPs through various Sponsors • In depth therapeutic and protocol knowledge as per Sponsor’s assignment. Excellent organizational and problem-solving skills.

Ideal Companies: Biotech companies

Tags for this Online Resume: research associate, biotech, CRA, Las Vegas, pharmaceutical, health

Featured Profile

Featured Profile

Dependably Organized

Energetic hard working Individual that is dependable, honest, as well as a fast learner, wonderful communication skill, team player, Very knowledge in many fields

Ideal Companies: Anything

Tags for this Online Resume: administrative

Clinical Research, Raleigh

To Obtain a position congruent with my education and level of experience in the Clinical Research field.

Tags for this Online Resume: Clinical Research Associate, Clinical Research Associate, ICH-GCP Guidelines, ICH-GCP Guidelines, Source Verification, Source Verification, Regulatory Document Maintenance, Regulatory Document Maintenance, Site Initiation Visits, Site Initiation Visits, Drug Accountability, Drug Accountability

Featured Profile

Nurse Manager 10 years experience

A dedicated professional, I have more than 26 years of experience and have played variety of roles as that of staff nurse, community leader, manager, and educator.Throughout my career, I have adapted to and maintained accepted standards and procedures. . I stay abreast with the current best practices and processes followed across various organizations.

Tags for this Online Resume: Medical Management , Nursing , Coordinator, Research, Educator, Team Leader, Cardiology, Hematology, Immunology, Management

Associate Logistics Coordinator 6 years of experiencia pharmaceutical industry

Natalia is a Biologist by profession; she graduated from Pontificia Universidad Javeriana in 2008 and her experience starts in 2007 where she did her practice in Brazil at Pontificia Universidad Catolica de Minas Gerais. In 2008 she joined Merck Sharp & Dohme and worked in Clinical trials as Assistant Data Coordinator, in 2011 she was promoted to Pharmacovigilance as Associate Data coordinator until 2012. Natalia Gómez is ...

Registered medical assitant/lead research study coordinator

I'm a Registered Medical Assistant/ Lead Research Study Coordinator. I have been a RMA for 5 years, in research for 3 years. I have experience in data management, drug accountability, people skills.

Tags for this Online Resume: Battle Creek , MI, Clinical , Research, Medical, Kalamazoo, MI, Medical Assistant

Sales Representative - 20 Years of Experience - Near 60453

sales/mangement position in the consumer packaged goods arena,calling on and managing retail grocery,mass-merch,drug accounts.

Tags for this Online Resume: sales manager, territory sales manager, Customer Relationship Management, Health Insurance, Inside Sales, Insurance, Retail, Sales, Cold Calling, Advertising

Clinical Research Associate

SUMMARY: To apply my knowledge of FDA Good Clinical Practice guidelines/ICH guidelines, extensive site/field Clinical Director, Site Lead Study Management, in addition to my experience with various therapeutic areas of medicine, to a position as a Clinical Research Associate. AREAS OF EXPERTISE * Management * Interview candidates and either make a selection decision or recommend individuals for hire. * Able to manage multip...

Tags for this Online Resume: Clinical Research, Research, Accounting, Acquired Immune Deficiency Syndrome (AIDS), Advertising, Amazon Elastic MapReduce, Audit, Basic First Aid, BLS, Budgeting

Clinical Regional Monitoring - 18 Years of Experience - Near 08053

Tags for this Online Resume: Clinical Research, monitoring, Cancer, Prestudy, initiation and close out visits, Inflammatory Diseases, Cardiovascular, regulatory review, Good Clinical Practices, New Jersey, Phase I - III Clinical trials, EDC, drug accountability, infectious diseases, laboratory and study supply, IRB documentation