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Online Resumes with "Clinical Trial "



Clinical Pharmacovigilance/Drug Safety - 17 Years of Experience

Summary: Over 16 years of Drug Safety experience that includes Global Drug Safety project management in Clinical Research Organization and Sponsor (Pharmaceutical) environments. Experienced clinical trial and post-marketing studies. Participated in stand-alone and full service studies as Global Drug Safety/Pharmacovigilance Lead in addition to mentoring and managing a team of junior drug safety associates.

Tags for this Online Resume: Oncology, Hepatitis, Query, Cardiovascular, Documentation, Infectious Diseases, Quality, Quality Assurance, Quality Control, Data Entry

Clinical Research - 9 Years of Experience - Near 38654

Career Summary Pharmacovigilance Director of consumer care division with an in-depth knowledge of Food and Drug Administration (FDA) regulations governing the reporting of adverse events and experienced in a GMP, compliance-driven environment. An articulate and positive communicator with proven effective management of staff, workload, vendors and associated processes to maintain exceptional quality, consistency and complian...

Tags for this Online Resume: Documentation, Management, Regulatory Affairs, Compliance, Integrate, Outsourcing, Quality, Risk Management, Triage, Audit, pharmaceutical, regulatory, Drug safety, clinical trials, research

Clinical Research - 3 Years of Experience - Near 30039

Tags for this Online Resume: Health Care Industry, Medical, Medical Records, Accounts Payable, Accounts Receivable, Complaints, Filing, Inventory, Payroll, Pricing, clinical, research, clinical trials

Featured Profile

Clinical Research Professional

I am looking for a career opportunity in research or any science related field.

Ideal Companies: Any research company, FBI, CIA

Tags for this Online Resume: clinical, research, project management, biology, medical , science, monitoring, clinical trials, regulatory, quality assurance, laboratory

Sales Manager - 7 Years of Experience - Near 27502

Certified SAS Base programmer * Knowledge of SAS programing techniques and programs with SAS Base and SAS Enterprise Guide * Basic concepts and knowledge in pharmaceutical industry and clinical trial, such as CDISC (ODM, SDTM, ADaM) * Proficient in creating and maintaining many datasets using Array, Merge, Update, Set and Proc SQL. * Proficient cleaning data using proc print, proc freq, proc univariate, proc means and proc ...

Tags for this Online Resume: Services, Management, Payroll, Retail, PeopleSoft, Sales, Inside Sales, Kronos, Kronos (Labor Mgmt Sys), People Skills, sas, sql, macro, SAS Base 9.4, SAS Enterprise Guide

Clinical Research

AREAS OF EXPERTISE * Clinical Trial Design * Biologics * Study Management * Medical Devices * Scientific Research * Regulatory Submissions * Program Development * KOL Relationships * Scientific Strategy * Oncology * Regulatory Strategy * Cardiovascular * Investigator Recruitment * Gastrointestinal * International Clinical Trials * Regenerative Medicine * Data Analysis * Surgery

Tags for this Online Resume: Clinical Research, Research, Pathway, Protocol, Regulatory Affairs, Infrastructure, Pharmaceutical, Publications, Selenium, Venture Capital, oncology, phase, clinical, gcp, protocol, trial, pharmaceutical, ich

Clinical Research - 14 Years of Experience - Near 35205

Career Highlights

Tags for this Online Resume: Cancer, Coding, Management, Medical, Medical Records, Policies and Procedures, Protocol, Research, CERNER, Communication Skills, clinical trials phase i

Clinical Data Management - 1 Years of Experience - Near 02176

SUMMARY: 4 years of experience in working with both Sponsor and CRO industry focusing on computer systems validation, query management and clinical data management documentation. Worked on creating and handling validation master plan, data management plan, case report forms, change control and data validation specifications. Experience in validation of software's of clinical trial databases, ePRO-electronic patient reported...

Tags for this Online Resume: Documentation, CFR Part 11, Management, Test, Test Scripts, Data Management, Hematology, User Acceptance Testing, Acceptance Testing, Change Control

Clinical Research - 20 Years of Experience - Near 11230

SUMMARY Senior medical professional with over 20 years of medical research experience and over 10 years managing clinical trial operations (Phases I - IV). I currently manage a team of over 25 medical/research professionals overseeing 15 concurrent trials. I am seeking a role where I can continue building on a career managing clinical trial operations on a larger scale.

Tags for this Online Resume: Medical, Pharmaceutical, Pharmaceutical Industry, Assessments, Clinical Research, Research, Documentation, Management, Ras, Training, trial, clinical, phase

Mental Health Therapist - 16 Years of Experience - Near 72034

Tags for this Online Resume: Medical, Medical Records, Patient Care, Management, AR, Behavioral Health, Computer Aided Software Engineering, Infection control, Policies and Procedures, Quality, RESEARCH, CLINICAL TRIALS, THERAPIST, GROUP, INDIVIDUAL, MANAGEMENT, TRAINING, EDUCATIONAL, CONSULTING, COUNSELING

Health Technologist - 1 Years of Experience - Near 08820

Summary * Certified Statistical SAS Base Programmer for SAS 9.4 with an overall experience of around 3 years working with SAS and SAS tools emphasizing on analysis, program development, QC and validation in life science and healthcare industries. Worked in Phase I- IV of clinical trials and has good knowledge in the presentation of the results in the standard formats * In-depth knowledge of SAS programming, data processing,...

Tags for this Online Resume: Programming, SAS, Active Directory Application Mode (ADAM), Base SAS, Collection, Data Analysis, Data Entry, Data Processing, Debugging, Engineering, CDISC, ADaM

Clinical Data Management - 17 Years of Experience - Near 80023

To manage clinical trials projects and a project management level by delivering clean and on-time and within budget. To collaborate with multiple internal / external parties to achieve excellent year-over-year results.

Tags for this Online Resume: Management, Data Management, Reviews, Process Improvement, Protocol, Quality, Documentation, Process Improvements, Query, Oncology, oncology, phase, clinical, trial, gcp, protocol, sas