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Online Resumes with "clinical trials "
Admissions Director
Tags for this Online Resume: pharmacist, clinical pharmacy, pharmacy manager, clinical trials, oncology pharmacy, ambulatory care pharmacy
Experienced Project / Safety Coordinator
To secure a challenging position in which my abilities and experience will be of value to an organization offering the opportunity for increased responsibility and knowledge.
Ideal Companies: Duke Univeristy, Merck & Co, Pfizer
Tags for this Online Resume: drug safety, clinical, research, coordinator
Pharmaceutical professional with 16 years experience
I am interested in positions in the NJ area in the following categories: Clinical Trial Management, entry level CRA, Clinical data management, Screening compound collection/data management, compound management. I am immediately available to begin work in any of the above positions
Tags for this Online Resume: Clinical Trial management, Clinical Data Management, Compound management, Biological data management, Screening library management, Clinical Research Associate
Masters student looking for entry level opportunities
I Aspire to obtain a job to gain experience the field of Regulatory Affairs in an organization, which provides a challenging working atmosphere in the Pharmaceutical Industry with an innovative & demanding job which would expand my knowledge and build my skills, along with the progress of the company.
Tags for this Online Resume: Healthcare, clinical trials coordinator, regulatory affairs specialist, qulaity assurance coordinator, drug safety associate, clinical research associate
Business Development Professional - 15 years experience Clinical Trials & Pharma
To obtain a Business Development postion within healthcare, pharmaceutical/biotech or medical device organizations with an opportunity for upward mobility.
Tags for this Online Resume: Business Development, Territory Sales
Clinical Trial Monitor/Manager - 6.4 yrs experience in Clinical Trial monitoring.management. Therapeutic expertise: Oncology. Others: GI, Resperitory, CVS, Nephrology, Endocrinology.
My Career Objective: To contribute my best of knowledge and skills in the field of Clinical Research to an excelling Pharma/CRO company which conducts quality and ethical clinical trial as per GCP guidelines. Also to bring profit to the company in drug development & pahrmaceutical market by timely delivery of quality work. I also strive to enhance my knowledge and skills and excel in career at all level.
Tags for this Online Resume: Sr. CRA, Clinical Team Lead, CRA, Clinical Trial Assistant, Clinical Project Manager
Clinical Specialist
Tags for this Online Resume: Clinical Trials, Research , Clinical Specialist
drug safety/pharmacovgilance/medical writing-9 years experience-global pharmaceutical
Objectives: To seek a growth opportunity in US pharmaceutical industry, a role in clinical research areas such as Drug Safety/Pharmacovigilance, Medical Writing, and Medical affairs.
Tags for this Online Resume: drug safety, pharmacovigilance, medical writing, clinical research, clinical trial or study, managerial/supervisory experience, senior level in global pharma company, risk management, US work authorization, GCP, FDA, ICH, detail-oriented, results driven, drug , medical , safety, clinical, writing, FDA, GCP, ICH, senior, regulatory, responsible, pharmaceutical
Clinical Trial Associate
Expand knowledge in Clinical Research Arena
Tags for this Online Resume: Research Assistant, Clinical Research Associates, Lab Technician, Research Associate
Clinical Regulatory Affairs
Tags for this Online Resume: Clinical research associate, clinical trials, clinical trials coordinator, regulatory
Vice-President Regulatory Affairs
To oversee regulatory affairs, write and/or review all documentation required by regulatory authorities for the conduct of clinical trials and for NDA approvals. To provide regulatory guidance and stratagies.
Tags for this Online Resume: regulatory affairs, QA/QC, clinical, management
Clincal Research Coordinator, Philadelphia
I would like a position that uses my knowledge and skills in clinical research to ensure the quality and intergiry of clinical trials.
