Assist clinical research coordinators in the conduct of clinical trials. Responsibilities include but are not limited to:

• Assist in preparation for study visits
• Assist in the collection of clinical data
• Enter data into EDC, CTMS
• Blood draws (phlebotomy) & specimen processing
• Assist with ancillary scheduling

Other Tasks:

• Collect clinical data: vital signs & ECGs, telephone calls and entering data into electronic data system
• Screening and enrolling study subjects based on inclusion/exclusion criteria
• Verifying study documents

• Experience interacting with patients
• Clinical research experience preferred
• Knowledge of medical terminology and laboratory skills preferred
• Knowledge of Microsoft Office required
• Excellent interpersonal and communication skillsinteract effectively with patients, staff, sponsors, and others as required.
• High attention to detail
• Ability to set priorities and meet deadlines
• Ability to work as a member of a team
• Possess well-developed interpersonal skills and an ability to work well independently, as well as with co-workers, peers, supervisor and external customers
• Able to maintain confidentiality with HIPAA guidelines, patient information and other sensitive information
• Demonstrate professionalism, sense of urgency and self-motivation to achieve required metrics

At Headlands Research, we are building a best in class clinical trial network. Were 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.