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Clinical Researcher Resume Examples

Clinical Researchers run clinical trials to test drugs for effectiveness and safety. They are typically involved in all stages of the clinical trial and complete duties such as writing trial protocols, designing data collection forms, collaborating with the ethics committee, setting up trial sites, closing down trial sites, and archiving study documentation. Based on our collection of resume samples for Clinical Researcher, main job requirements are knowledge of clinical trial procedures, organization, accuracy, being able to motivate others, multitasking, an eye for details, and computer competences. Employers choose resumes displaying a postgraduate degree in medical sciences, life sciences, or nursing.

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Clinical Researcher Resume Samples

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Candidate Info

3

years in workforce

1

year at this job

BS

Biomedical Engineering

Clinical Researcher

Researched and studied the effects of Forteo and Bisphosphates on osteoporotic, human bone.
Authored SOP and developed techniques for Fuchsin staining, microtome prepping, and analyzing biopsies.
Analyzed bone properties using OsteoMeasure software and standard microdamage microscopic techniques.
Presented Forteo findings at 2016 Clinical and Translational Science conference in Lexington, KY.

Candidate Info

5

years in workforce

5

months at this job

BS

Business Administration

MA

Epidemiology & Public Policy

Senior Clinical Researcher

Analyzes highly complex data gathered on clinical research for Pediatric Allergy studies.
Coordinated SAE reconciliation between the safety database and clinical databases at multiple data management vendors according to timelines set for milestones of the clinical trials.
Ensured that all projects are delivered on-time, within the scope and the budget
Developed a detailed project plan to track progress
Ensured that the Delegation Logs are updated and signed from all fellows, PI’s, and Research Coordinator
Oversees data collection, processing, storage, inventory and quality control for clinical research studies.
Coordinated protocols and human subject approvals between various sites.
Assisted the Principal Investigator and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials.
Measured project performance using appropriate systems, tools and techniques.

Candidate Info

3

years in workforce

2

years at this job

BS

Bachelor of Science

Clinical Researcher/sourcing Specialist

Search, identify, and qualify all candidates sourced via job boards, social media, cold calls, etc.
Build and maintain candidate pipelines for current and future jobs.
Interview and travel coordination.
Manage jobs and candidates in our ATS.

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