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Online Resumes with "Good Clinical Practice"




Regulatory Compliance Specialist

Ideal Companies: MedImmune, NIH, Social & Scientific Systems

Tags for this Online Resume: triage, clnical trials, auditing, informed consents, study protocols, communications

Extremely detail oriented Clinical Research Manager

Experience in multi-areas of research from inception to closeout with special emphasis on compliance with FDA regulations and good clinical practices

Ideal Companies: Quintiles PPD ICON Clinical Research Radiant Research

Tags for this Online Resume: Clinical Research Coordinator, Research regulatory Specialist, Clinical Research Manager

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

Experienced Data Coordinator Relocating to Dallas, Texas

I am looking for a company where I can add to my extensive list of Data Coordinator skills as well as share my skills with others. Working for a company which fosters the expansion of knowledge, is constantly growing and supports its employees is very important to me.

Tags for this Online Resume: SAS, eDM, Oracle Clinical, DMP Composition, CRF Completion Guidelines Composition, External Data Reconciliation, Multi-tasker

Featured Profile

I have both hands-on and clinical experience in the medical field, as well as familiarity with FDA regulations GCP,GLP, Human Safety issues, Clinical Protocol Design and Clinical Trials design. I also have MSL ( Medical Science Liaison ) experience in di

I am looking for a MSL position,be able to utilize my experience providing leadership to develop a team to increase in sales,service quality and long term organizational stability to increase profits.Be able to communicate at all levels nationally and internationally

Ideal Companies: Amgen, General electric. Alcon Allergan, any pharmaceutical or medical device company

Tags for this Online Resume: MD, consultant, clinical trials, protocol design SOP, GCP, GMP, SOP, fluent English, Ophthalmologist, willing to travel, willing to be relocated, fluent Spanish, fluent Italian, Latin America, American Citizen, medical liaison

Looking for exciting and challenging career in Clinical Research

Dedicated professional with comprehensive academic and professional background. Committed to career in clinical research and is looking for a CRA or assistant clinical project manager position. Outstanding interpersonal, facilitation, and communication skills. Possess extensive experience in the pharmaceutical industry in performing in-house monitoring activities related to phase I-IV clinical trials with emphasis on the fo...

Ideal Companies: Pharmaceutical/Biotech industry

Tags for this Online Resume: clinical research, medical affairs, Clinical research Associate, Clinical Research Assistant, Clinical Development Associate, Clinical Development Assistant, Regulatory Affairs Associate, Regulatory Affairs Assistant, Drug Safety Associate, Drug Safety Assistant, Clinical Development, Clinical Trials Associate, Clinical Trials Assistant

Clincial Trial Management

A challenging position, with salary commensurate with the job responsibilities and my education & experience.

Tags for this Online Resume: project management, data cleaning, data workflow, good clinical practices, data management, clinical trial, database, oracle clinical

Featured Profile

For the past 4 years I have been working as an Aerotek Contract Clinical Document Specialist at Otsuka assisting with all document aspects pertaining to a clinical trial.

In a new job I am looking for the opportunity to contribute and be a part of an organizations team and not just be considered as a contractor or temporary professional. In my past four years at Otsuka I have assisted with all document aspects that pertain to a clinical trial and have the experience and no how to provide the following to any organization: ï‚§ Hands-on experience supporting Clinical Research Assistants...

Ideal Companies: Medium size bio-tech company

Tags for this Online Resume: Auditing, Proofreading, Manage Complex Data, Accurate Documentation, Clear Communicator

Featured Profile

Clinical Research Coordinator - 8 years experience - Oncology

I am seeking a position in clinical research coordinating complex clinical trials, preferably in oncology. I would also be interested in a position as a Clinical Research Associate with a pharmaceutical company or CRO.

Ideal Companies: Large pharmaceutical company

Tags for this Online Resume: Good Clinical Practice, CRF, SAE reporting, Consent process, IRB , ICH

Starting out in Clinical Research

I know biology. I know bioethics. I know good clinical practices. Now, I want to do them.

Ideal Companies: University of Chicago, Northwestern University, University of Illinois at Chicago, Rush University

Tags for this Online Resume: Research, Clinical, Data

Responsible and able to work under presure.

High energy with interperonal, communication and leadership skills. Resourceful and very responsible

Ideal Companies: Laboratory, enviromental, Public Health, Customer Service

Tags for this Online Resume: research assistant, administrative assistant, customer services, research technician, case manager