Clinical Research Coordinator

Job Description Summary: The Clinical Research Coordinator (CRC) works under the direction of company administration and the principle investigator to perform assigned and delegated duties associated with the execution of clinical research trial protocols. The Clinical Research Coordinator will have, or will develop, skills in phlebotomy, electrocardiograms, collection of medical/surgical histories, basic laboratory tests, performance of subject trial visits, completion of case report forms (CRFs), and resolution of data queries. The Clinical Research Coordinator will participate in the completion of regulatory documents. The Clinical Research Coordinator shall have the highest moral and ethical standards and will be expected to conduct themselves in a responsible, professional, moral, and ethical manner at all times. The Clinical Research Coordinator shall have excellent interpersonal communication skills and have a strong commitment to the success of the research team.

CRC Responsibilities:

- Assist in the coordination and execution of clinical drug trials under the guidance and direction of the site administrator, principal investigator, and sub-investigators.

- Read, comprehend, and execute clinical trial protocols.

- Perform laboratory tests as required by trial protocol.

- Monitor clinical and laboratory data for accuracy and compliance with trial protocols.

- Complete all documentation required by trial protocol for submission to the trial sponsor.

- Comply with all international, federal, state, local, and company guidance, laws, regulations, policies, and procedures as applicable to clinical research trials and Advanced Research Institute.

- Interact with patients by explaining trial protocols, consenting subjects, monitoring their compliance with protocols, collecting data, and collection laboratory samples.

- Protect every subject's safety to the best of your ability.

- Maintain every patient's rights to privacy.

- Maintain flexibility by performing all other assigned duties.

-Perform phlebotomy. (Phlebotomist.)

Training: On the job training. Formal continuing education opportunities provided.

Experience Requirements: Experience is highly preferred but not necessarily required.

Education Requirements: High school diploma required.

Job Type: Full-time

Schedule:

• 8 hour shift
• Monday to Friday
• No weekends

Ability to commute/relocate:

• Tigard, OR 97223: Reliably commute or planning to relocate before starting work (Required)

Education:

• High school or equivalent (Required)

Experience:

• Research: 1 year (Preferred)
• Clinical trials: 1 year (Preferred)
• Phlebotomy: 1 year (Preferred)

Work Location: In person

Job Type: Full-time

Pay: $22.00 - $27.00 per hour

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Flexible spending account
• Health insurance
• Paid time off

Ability to Commute:

• Portland, OR 97223 (Required)

Work Location: In person