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Online Resumes with "GCP"



Clinical Research Manager, Atlanta- 22 years expertise

Manage a clinical research team or project to on-time, quality deliverables.

Tags for this Online Resume: Project Nanager, Project Manager, CRA Manager, GCP Auditor, GCP Trainer , Lead CRA, Medical Writer, Associate Director

Post doctoral Research Fellow, Research physician

Respected Sir, I am a medical doctor with more than ten years of experience and currently exploring the job opportunities in the field of pharmacovigilence and / or drug safety. As my resume reveals, I have Bachelor’s in medicine and surgery and my master in public health. I enjoy working in a high energy and high performance work environment. Currently I am running post market clinical trials in USA. I have ample experie...

Tags for this Online Resume: Post-doctoral Research fellow, Research physician, Pharmacovigilence deptt, Drug safety, Epidemiologist

Clinical Research Professional, San Francisco Bay Area

Established reputation as a highly motivated and productive professional in the CRO/Pharmaceutical/Biotechnology industry. Able to quickly and thoroughly gain expertise in a particular field and integrate new information with the existing knowledge. Capable of identifying and solving complex problems in creative and logical ways. Adept at combining critical solutions with imagination, innovation, and a sense of humor. ...

Ideal Companies: Stanford, Palo Alto Medical Foundation, Jazz

Tags for this Online Resume: All Database Knowledge, Excel, Microsof, ICH/GCP Compliant, Vendor Oversight, CTMS, Trial Master File, medical Device

Clinical Research Associate, Boston

 To acquire a position as a Clinical Research coordinator in a pharmaceutical company or a CRO that will benefit from my skills, knowledge, experience and enthusiasm and that will give me an opportunity to learn and grow further.  To be responsible for the administration, initiation and monitoring of the Clinical research project in accordance with the FDA regulations and ICH-GCP guidelines.

Tags for this Online Resume: clinical research assistant, data administrator, regulatory affairs assistant, CRA, Drug safety associate, Quality Assurance, clinical research associate

Certified Clinical Research Associate

I am aspiring to enrich my clinical professional experience to improve the lives of others I am an ASCP certified Medical Technologist with extensive compliance and regulatory experience gained through working with the Texas Department of State Health Services CLIA division as an auditor.

Tags for this Online Resume: CRA, GCP, Regulatory Affairs, Clinical, Laboratory, Compliance

clinical research associate

To achieve excellence in working as dynamic professional offering solutions to business using the best available where my analytical ability and analysing quest are used maximum for growth of the organization and to grow with the organization. Seeking a challenging position in well established company that offers professional growth and ample opportunity to learn and enrich my competencies in my profession.

Tags for this Online Resume: monitaring, gcp, quality assurence

Clinical Quality Assurance

Looking for a challenging career in auditing in clinical research field.

Tags for this Online Resume: GCP Auditor, ICH GCP, Quality Management System, Investigator Site Audits, Audits in MENA, Asia Pac, Vendor Audits

Clinical Research, Research Triangle Park

Savvy, analytical, highly organized and detail oriented individual in search of an interesting position within the realm of clinical trials research. Ideally, the position would allow me to take advantage of my understanding of biology, research methodology, experimental design and medical terminology. I am seeking a position that will lead to a clinical research associate position.

Tags for this Online Resume: Oncology, Clinical Trials, Analytical , Research, GCP/ ICH

Clinical Research Professional, Charlotte, ICH/GCP/FDA Trained

Tags for this Online Resume: GCP, ICH, 21 CFR 50, 21 CFR 56, 21 CFR 312, 21 CFR 812, 45 CFR 46, Medical terminology, Data management, Project development, Site monitoring, CRA, CRC

Featured Profile

Drug Safety / Pharmacovigilance - RTP, NC

Dynamic, enthusiastic, and performance-driven Doctor of veterinary medicine intent on transferring 10 years of knowledge and experience in a clinical setting to a challenging career working in the Pharmaceutical or Contract Research Organization industry with a progressive company offering opportunities for growth and advancement. Outstanding team player and communicator with highly detailed documentation skills seeking t...

Tags for this Online Resume: Medical terminology, ICH/GCP guidelines, DIsease states, Pharmacology, Customer service, Medical writing

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