Cannabis jobs at SF Research Institute Inc.

CLINICAL RESEARCH COORDINATOR - Work on a project basis OR on contract OR part-time. Assigned to a specific study.

Pharmacokinetic experience is preferred. Cannabis research is a plus.

Prefer SITE experience

Administratively and clinically manage multiple clinical trials (Pharmacokinetics.)

Responsible for trials from beginning to end (hands on and all encompassing)

Coordinate all aspects of the project, including study staff and study schedule and timeline

· Adhere to Research SOP’s
· Adhere to Good Clinical Practices and the study protocols
· Ensure scientific integrity of data and protect the rights, safety, and well-being of patients
enrolled in clinical trials
· Discuss study protocols with patients and verify the informed consent documentation
· Provide patient with written communication of their participation (i.e. copy of the signed
informed consent)
· Ensure patient’s referring physician receives notification of patient’s participation in
studies as requested by the patient
· Meet with patient for each visit and maintain accessibility to discuss any
questions/concerns regarding the study
· Dispense investigational product in a professional and accountable manner following protocol
requirements
· Oversee staff to Collect specimens at scheduled patient visits and vitals when necessary
· Schedule all patient research visits and procedures consistent with protocol
requirements
· Complete and maintain case report forms per FDA guidelines, and review them against
the patient’s medical record for completeness and accuracy

Ensure that non-serious and serious adverse events are properly documented and
reported
· Screen all laboratory results when received and follow protocol procedure regarding
abnormal results
· Ensure all laboratory results are given to appropriate doctors for review of clinical
significance, then file results in the patient study binder
· Submit patient reimbursement requests at the conclusion of patient’s participation in
protocol
· Ensure the filing and maintenance of all regulatory documents

· Prepare Site Qualification documents
· Schedule and prepare SIV and monitor visits and set up for monitoring visits prior to monitor’s arrival
· Other duties as assigned.

Job Types: Full-time, Part-time, Contract

Ability to commute/relocate:

• San Francisco, CA 94127: Reliably commute or planning to relocate before starting work (Preferred)

Work Location: One location

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