- Overseeing the smooth running of clinical trials.
- Electronic Data Capture using numerous online portals.
- Informing participants about study objectives.
- Administering questionnaires.
- Monitoring research participants to ensure adherence to study protocols.
- Adhering to research regulatory standards.
- Adhering to ethical standards.
- Maintaining detailed records of studies as per FDA and HHS guidelines, including things such as drug dispensation and inventory.
- Liaising with laboratories regarding findings.
- Participating in subject recruitment efforts.
- Ensuring that the necessary supplies and equipment for a study are in stock and in working order.
- Engaging with subjects and understanding their concerns.
- Diagnostic Imaging.
- Medical history review.
- Collecting, coding, and analyzing data obtained from research protocols.
- 2+ years in healthcare, ophthalmology preferred.
- Analytical mindset.
- Attention to detail.
- Exceptional interpersonal skills.
- Outstanding written and verbal communication.
- Excellent organizational skill.
- Willingness to continually self-educate.
- IATA certification within 60 days
- Must possess the physical, mental, and cognitive skills needed to complete essential tasks, including abilities such as learning, remembering, focusing, categorizing, and integrating information for comprehension, problem-solving, and timely decision-making.
- High School Diploma or equivalent required.
- We are willing to provide training.
- Sitting, Standing, Bending, Reaching, Stooping, Walking and Lifting
- Ability to see, hear, and speak with sufficient capability to perform assigned tasks.
- Driving independently to other facilities
- Work may involve a high level of stress.
- Occupational Exposure - Category Ill exposure to blood-borne pathogens and may encounter chemical hazards.
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Clinical Research Coordinator - North Dartmouth, United States - Claris Vision
Description
We are looking for candidates with medical backgrounds and excellent interpersonal skills for the position of Clinical Research Coordinator. Clinical Research Coordinators are responsible for administering questionnaires and subject material, adhering to regulatory trial protocol standards and participating in subject recruitment efforts, among other duties.
*** This is onsite in Dartmouth, MA ***
Duties/Responsibilities:
Required Skills/Abilities: