Clinical Research Coordinator I

ObjectiveHealth-posted about 2 months ago

Full-time • Entry Level

South Bend, IN

101-250 employees

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Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator. The ideal candidate will possess certification such as an MA, phlebotomy, or similar and have a strong desire to work directly with patients.

Conducting all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients.
Performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG, etc.
Maintaining clean data entry, regulatory compliance, productive site visits, efficient study set-up and maintenance, and strict protocol adherence.
Communicating effectively with the research team, PIs, Sponsors, Monitors, and others.
Tracking AE and SAE events, and maintaining eSource material for assigned studies.

Certification such as an MA, phlebotomy, or similar.
Strong desire to work directly with patients.
Acute attention to detail.
Ability to stay focused while managing multiple protocols.
Expert communication skills.

Experience in clinical research or related fields.
Familiarity with technologies used in clinical research.

Competitive compensation.
401(k) with Company match.
Clear career pathway for advancement within the Company.
Short- and Long-Term Disability.
Health Savings and Flexible Spending Accounts.
Health, Dental and Vision insurance Plans.
Generous PTO.
Adoption Assistance.
Paid Holidays.
Wide selection of other voluntary benefits.

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Clinical Research Coordinator I

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