Overview:
At Headlands Research, we are building a best in class clinical trial company. 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 18 clinical trial sites in the US and Canada and have rapid expansion plans.
The Role
Headlands Research Brownville is looking for a Clinical Research Assistant to assist coordinators in 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.
Responsibilities:
- To assist research coordinators in conducting clinical trials. Responsibilities include but are not limited to:
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Collect clinical data: vital signs, telephone calls and entering data into electronic data system
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Screening and enrolling study subjects based on inclusion/exclusion criteria
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Verifying study documents
Qualifications:
- Clinical research experience preferred
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Knowledge in medical terminology and laboratory skills preferred
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Knowledge with Microsoft office required
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Excellent interpersonal and communication skills—interact effectively with professional, administrative staff, sponsor and regulatory representatives, patients, potential subjects, and referral sources
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Accuracy, attention to detail and ability to set priorities and meet deadlines