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Form of work
SalaryOverview:
Together with Headlands Research, we are building a best in class clinical trial network. We’re an exceptional family of next-generation clinical trial sites, integrating cutting edge technology and high-quality support services, and significantly expanding participant engagement Founded in 2018, our company operates 18 clinical trial sites in the US and Canada with rapid plans for expansion.
The Role
Headlands Research 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:
Qualifications:
Peninsula Research Associates (PRA) is a trailblazer in advancing medical treatments through innovative techniques and groundbreaking research. With significant study results in allergy, asthma, vaccines, otitis media, and sinusitis treatment, we have earned a reputation for excellence in the field.
Together with Headlands Research, we are building a best in class clinical trial network. We’re an exceptional family of next-generation clinical trial sites, integrating cutting edge technology and high-quality support services, and significantly expanding participant engagement Founded in 2018, our company operates 18 clinical trial sites in the US and Canada with rapid plans for expansion.
The Role
Headlands Research 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:
- 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
Qualifications:
- Clinical research experience preferred
- 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
