Job Description
The Clinical Research Assistant (RA) is a research professional working with and under the direction of the clinical research site management, Principal Investigator (PI), and clinical research staff.
The Research Assistant supports the clinical research staff with daily clinical trial activities which may include phlebotomy, laboratory, data entry, and administrative assignments.
Essential Duties and Responsibilities :
- Work with site management and monitoring efforts to ensure protocol adherence.
- Assists with coordinating and facilitating monitoring visits.
- Prepares study materials for assigned studies.
- Assists with organizing study files.
- Performs study-related procedures according to study protocol as trained (i.e. Vital signs, ECG, phlebotomy, pulmonary function testing, urine pregnancy, and drug testing, processing blood, or any other procedures required per protocol or ordered by study investigator).
- Collects data on source documentation as required by the protocol.
- Maintain regulatory files throughout the conduct of the entire trial.
- Reviews study supply inventory to ensure the site has an adequate inventory of all study supplies.
- Works with the lead study coordinator to assist with resolving any issues that may arise during the conduct of the study or during a monitor visit
Qualifications
Requirements :
- Certified Medical Assistant or Licensed Nurse preferred
- Excellent verbal & written communication skills
- Ability to learn quickly, read and understand complex protocols, follow very detailed directions, and multi-tasking
- Must be able to maintain strict confidentiality of patients, employees, and company information at all times and adhere to HIPAA Guidelines
Additional Information
A career opportunity with M3 Wake Research offers competitive wages, and benefits such as :
- 401(k), 401(k) matching
- Dental insurance
- Disability insurance
- Employee assistance program
- Flexible spending account
- Health insurance
- Life insurance
- Paid time off
- Vision insurance
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