At Headlands Research, we are building the best clinical trial company in the world. We’re an exceptional family of next-generation clinical trial sites, integrating cutting edge technology and high-quality support services, and significantly expanding participant outreach and participation. Founded in 2018, our company is in high growth mode; we operate 15 clinical trial sites in the US and Canada and have rapid expansion plans.
The Role
Headlands Research is looking for a Research Assistant to assist coordinators during clinical visits for clinical research protocols. This individual will work directly with the coordinators, investigators, and other research staff to ensure protocol visits are being completed in accordance with protocol guidelines.
To assist research coordinators in conducting clinical trials. Responsibilities include but are not limited to
Collect clinical data vital signs, telephone calls and entering data into electronic data system
Screening and enrolling study subjects based on inclusion/exclusion criteria
Verifying study documents
Must be okay with blood and needles; this position will require phlebotomy certification within 6 months of hire.
Clinical research experience preferred
Conducting vitals, manual blood pressures, glucose checks, and additional clinical skills a huge plus.
Knowledge in medical terminology and laboratory skills preferred
Knowledge with Microsoft office required
Excellent interpersonal and communication skills—interact effectively with professional, administrative staff, sponsor and regulatory representatives, patients, potential subjects, and referral sources
Accuracy, attention to detail and ability to set priorities and meet deadlines
Seniority level
Entry level
Employment type
Full-time
Job function
Research, Analyst, and Information Technology
Industries
Research Services
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