Required Education:

CCRC certified/eligible.

Required Experience:

2 years as CRC is required.

Required Language:

Bi-lingual English/Spanish preferred.

Job Type: Full-time/Part - time

ESSENTIAL FUNCTIONS:

Supports enrolling participants on to clinical trials through recruitment, screening, enrollment and follow-up according to protocol requirements.
Responsible for working with the principal investigator to meet or exceed study enrollment.
Reviews the study design and inclusion/exclusion criteria with physician and patient.
Ensures the protection of study participants by verifying informed consent procedures and adheres to protocol requirements/compliance.
Ensures the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review. Monitors data for missing or implausible data.
Ensures the adequate and accurate records are maintained for inspecting.
Creates study specific tools for source documentation when not provided by a sponsor.
Collects and compiles and enters data into study specific CRFs or electronic data capture (EDC) systems.
Generates and tracks drug or device shipments and supplies as needed.
Reports and follow-up on serious adverse events as necessary.
Implements study-specific communications.
Ensures timely adherence to protocol requirements.
Responsible for completion of all required training and documentation according to site work guidelines.
Ensures timely and accurate data collection.
Maintains accurate and complete records including regulatory documents when applicable, signed informed consent forms, source documentation, drug dispensing logs, device utilization logs, subject logs, and study-related communications.
Tract and report adverse events, serious adverse events, protocol waivers, deviations, and violations.
Attends study-specific on-site meetings, Investigator meetings, and conference calls as required or directed by the sponsor.
Assists sponsor and US FDA audit teams as needed.
Maintains patient confidentiality according to ethical and legal requirements.
Assists in providing research coverage for clinics as needed.
To perform miscellaneous job-related duties as assigned

Job Type: Full-time

Required education:

Bachelor's

Required experience:

Healthcare: 2 year
Clinical Research: 2 year
Research: 2 year

Job Type: Part-time

Pay: $20.00 - $30.00 per hour

Education:

Bachelor's (Preferred)

Experience:

Research: 2 years (Preferred)

License/Certification:

CCRC certified/eligible. (Preferred)

Location:

Dartmouth, MA (Required)

Work Location: In person

AMAC Neurology

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