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Online Resumes with "Clinical studies"



“Why settle for the inexperience of youth? Work with one who has the maturity, reliability and experience you require.”

High energy manager/coordinator with a flair for creativity.

Ideal Companies: Medical Centers., Graphic design., Database creation.

Tags for this Online Resume: Medical Management/Coordinator

Cell biology scientist

•Exacting, highly organized researcher with more than 12 years of combined experience in the pharmaceutical industry and university-based clinical pharmacology settings. •Experienced in investigation of Mechanism of Action of novel immunobiologics in investigator-initiated and clinical studies using disease-related biomarker selection and analyses. •Strong background in designing and conducting studies pertaining to the ...

Ideal Companies: Biotech companies

Tags for this Online Resume: biomarkers, immunologist, skin, clinical pharmacology, NF-kappa B, signaling

Senior/Lead Clinical Research Associate

Seasoned Clinical Research Professional with 10+ years experience in Clinical Research, including, CRA, Lead CRA, and Project Management duties. THerapeutic areas include oncology, endocrine/metabolism, and CNS.

Ideal Companies: biotech, pharma

Tags for this Online Resume: clinical trials manager, oncology, clinical research

PH.D. scientist with 8 years experience in drug discovery and development and expertise in infectious disease

I am looking primarily for an associate director/director position in pharmaceuticals or biotech. I would also consider a senior scientist position. I prefer infectious disease drug discovery and/or development but would also consider other areas.

Ideal Companies: Nexbio, Regulus, Pfizer, Eli Lilly, Merck

Tags for this Online Resume: virology, infectious, discovery, therapeutics

Cross functional thinker and cross cultural team player

I thrive on learning new things and constant changes. Leading edge does not turn me away. Currently working in Switzerland and seriously looking to relocate to Asia for good opportunity.

Ideal Companies: Google, Nintendo, Goldman Sachs

Tags for this Online Resume: PMP, Big five, 21 CFR Part 11, GCP, GMP, CSV, Biotech, Clinical study planning and forecasting, Clinical investigator portal

Compassionate and Caring in the Mental Health Field

Ideal Companies: Research companies, State of Florida, Home Health agencies

Tags for this Online Resume: Mental Health, Clinical Research

Bilingual Clinical Study Associate

A proactive, results and details oriented leader.

I am looking for a job that will allow me to solve and troubleshoot customers' production problems proactively and creatively.

Ideal Companies: Company that will take care of emplyees ' well beings, always looks for ways to improve Employees'teamwork.

Tags for this Online Resume: COBOL, SAS, RATIONAL TOOL ClearQuest, DB2/SQL, VSAM/JCL, TSO/ISPF, IT Service Management, E-Collaborate, Documentum, Wiki, ASSEMBLER, BASIC, MS ACCESS, EXCEL, PROJECT, VISIO, WORD, UNIX, CASE TOOLS, HYPERION, INFORMATICA, CITRIX

Clinical Research Associate - 5 yearsexperience - Regulator Affairs

I am currently looking for an appropriate job opening in a Research Institute. I have five years experience as a Clinical Research Associate (as Regulatory Officer and Medical Writer). I had been working with reputed pharmaceutical companies in India. I have led a team of Medical writers and as a part of them, I have written Clinical and Pre-clinical overviews on more than 100 molecules for regulatory dossier submission ...

Tags for this Online Resume: Protocol Development, Clinical study report, Clinical study audit and monitoring, Regulatory dossier submission, RMP, PSUR, Leaflet, Regulatory queries

Postdoctoral Fellow

Career goals: Lead a bio-research team that evaluates development of new product/s, initiates research for clinical studies.

Tags for this Online Resume: cellular immunology, molecular biology, inflammation, pain, assay development, drug target

Expectional and Experience CRA - Certified CRA with 9 years experience - c

My career goal is to have an impact on the entire process of clinical studies. I would like to broaden my horizons beyond the normal CRA role performed and be involved in the entire clinical study from start to finish. I want to be involved in the protocol from beginning (developing the protocol) to the FDA submission. From my previous experiences I know I can have a positive effect on the successful outcome of studies.

Ideal Companies: Pharmaceutical companies, CROs

Tags for this Online Resume: Clinical Research Associate , CRA III, Senior CRA, Experienced, Contract, ex

Senior Technical Editor, Electronic Document Coordinator/Specialist