Supervises, designs, plans, and develops clinical evaluation research studies.
Prepares and writes protocols and patient follow-up forms.
Conducts registered and unregistered clinical studies on products that meet a medical need and/or have commercial potential.
Supervises and interprets the results of clinical investigations for new applications for medical devices, drugs, or consumer products.
Manages and resolves the operational aspects of clinical trials in collaboration with project teams and in accordance with standard operating procedures (SOP), Good Clinical Practice (GCP), and applicable country regulations; prepares clinical trial budgets.
Responsible for clinical supply operations, site selection, and vendor management.

Requirements

Master’s degree in clinical sciences or a related field.
In-depth knowledge of the field, typically gained through higher education complemented by professional experience.
Practical experience in project management.
At least 4 years of experience in clinical research.

Benefits

Competitive salary and a flexible benefits package
Recognition of employee contributions
Success-sharing with employees
Wide range of benefits and resources

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

clinical evaluation researchprotocol writingclinical study designdata interpretationclinical trial managementbudget preparationvendor managementsite selectionGood Clinical Practice (GCP)standard operating procedures (SOP)

Soft Skills

supervisory skillsproject managementcollaborationproblem-solvingcommunication