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Online Resumes with "study protocols"
Director / Manager Environmental Health and Safety
Expert in the fields of Environmental Health and Safety, Industrial Hygiene and Toxicology Have expertise and experience in the fields of Safety, Industrial Hygiene, Environmental Sciences, Toxicology, Manufacturing, Pharmaceutical Health, Safety, Research and Development. Have more than 8 years of experience in the health and safety field. In addition, have governmental and regulatory experience and have acquired more tha...
Ideal Companies: Merck, IBM, General Electric, Exxon, Johnson & Johnson, NYCDEP
Tags for this Online Resume: Environmental Health and Safety, Safety, Environmental Science, Pharmaceutical, Director, Manager, Coordinator, Regulations, OSHA, EPA, DOT, DEP, DEC, Industrial Hygiene, Toxicology
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 CRO management professional offering 20+ years of pharmaceutical toxicology experience
Looking for opportunities to excel in sponsor/CRO relationships. Last 10 years have been devoted to monitoring, managing, and building relationships with preclinical Contract Research Organizations (CROs) through demonstrated ability to plan, coordinate and interact professionally with all levels of staff both internally and externally. I possess excellent communication and interpersonal skills and have a firm understandi...
Ideal Companies: Biotech or pharmacuetical companies
Tags for this Online Resume: Preclinical Toxicology Outsourcing, Toxicology Account Manager, Preclinical Program Manager, Toxicology Study Monitor, Contract manager, CRO liason
Reimbursement Professional
I am looking for a position with an established medical device, pharma, or biotech company where I can enhance my knowledge and scope of responsibilities in the reimbursement field.
Ideal Companies: medical device, physicians, hospitals. Open to pharma or biotech
Tags for this Online Resume: Reimbursement, Payer, Revenue Cycle
Sr. Clinical research Associate/ Director of clinical research
Can undertake most of the tasks and works independently. Very much focussed on the timelines and quite goal tending. Willing to help others in their prioritized tasks. Excellent planning, design and implementation. Highly experienced in writing reports and data analyses.
Ideal Companies: Pharmaceutical industries, Biotech companies, Research institutes, hospitals and for profit mid to large companies.
Tags for this Online Resume: Director of clinical research, Manager of drug safety, Senior clinical research associate, Regional clinical research associate
Clinical Supplies Manager
Consistently produced investigational medicinal products within aggressive timelines and according to cGMP guidelines as required by study protocols. Strong Program Management skills with an emphasis on the design and forecasting of accurate drug demands for multiple ongoing global Clinical Trials. Proficient in communicating with a diverse group of people including team members and vendors. Achieved objectives through my ...
I am MD by background with more than 5 years of clinical research experience
I am looking for a challenging job in a team-oriented environment.
Ideal Companies: Allergan, Genentech, Ista, Santen
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
Clinical Study Associate, RTP
Lead clinical study associate with extensive experience in delivering clinical study support to internal and external research partners. Track record of ensuring adherence to study timeline and budget parameters and compliance with regulatory agencies, study protocol, and corporate / sponsor requirements. Demonstrated success implementing process improvements to reduce site initiation time and improve internal and study sit...
Tags for this Online Resume:  Project Materials Preparation / Review,  Team Supervision & Training,  Workload Planning,  Document Management / Auditing,  Timeline / Budget Management,  Clinical Supply Inventory Maintenance
Creative problem solver
Tags for this Online Resume: Medical Writing, Study Design, Data analysis
Diligent, engaging, and efficient Regulatory Affairs Specialist within the Medical Device Manufacturing Industry offering 8+ years of progressive experience and measurable accomplishments in the field. Expert at providing key leadership and training to st
In reviewing the attached résumé, you will note that I possess over 8 years experience assuming progressive roles from a Research Associate to an Associate Research Scientist. My keen knowledge and understanding of R&D and Regulatory Affairs to contribute to the design and preparation of non-clinical study protocols, as well as the design, initiation, monitoring, and close-out of studies for stability and validatio...
Tags for this Online Resume: Regulatory Compliance , Project Management, Technical & Report Writing , Data Analysis (Statistics & Charts) , Team Building & Leading , Staff Training & Development
