Clinical Research Nurse

Seattle Clinical Research Center is seeking a full-time Clinical Research Nurse to join our research team.

Seattle Clinical Research Center (SCRC) is a dedicated clinical trial investigative site. SCRC has successfully executed hundreds of multi-specialty Phase I-IV medical device and biopharma clinical trials since 1991 and has particular expertise in women’s health-related drugs and medical devices as well as migraine and vaccine studies.

The Clinical Research Nurse (CRN) serves as an integral member of the research team and will work closely with members of SCRC's staff across the organization. The CRN reports to the Lead Clinical Research Coordinator. The ideal candidate will combine clinical research experience with excellent communication skills and the ability to manage multiple projects with strong attention to detail. The CRN’s main responsibility is the conduct of multiple clinical trials. CRN’s will work closely with research subjects, the Principal Investigator, Sub-Investigators, and Sponsors/CROs to ensure that each study is conducted properly per protocol and Good Clinical Practice.

Job Responsibilities:

· Screening and recruitment of potential study participants

· Conducting informed consent discussions

· Collecting vitals and medical history

· Performing phlebotomy (if able) and administering SQ/IM injections as needed

· Tracking clinical trial subjects and scheduling follow-up assessments

· Completing and organizing regulatory documents

· Communicating with the Sponsor, CRO, & IRB

· Performing all coordinator-mediated tasks, per individual protocols

· Drug accountability and reconciliation

· Processing and packaging specimens, per IATA guidelines

In order to be successful at this position, you should:

· Be a licensed Registered Nurse in the State of Washington

· Have at least one year of experience as a Clinical Research Coordinator (CRC) or relevent experience

· Have experience with direct patient care, preferably in the field of women's health

· Have experience in conducting an informed consent discussion

· Have experience obtaining medical history and basic vital signs

· Be organized, flexible, and willing to step in where needed

· Have attention to detail

· Be self-motivated and a fast learner

Preferred requirements:

· Have a Bachelor's degree

· Phlebotomy experience

· Processing and packaging lab specimens in compliance with IATA guidelines

· Training in HIPAA, Good Clinical Practices (GCP) and Human Research Protection

Job Type: Full-time. 100% on site.

Job Type: Full-time

Pay: $72,000.00 - $90,000.00 per year

Benefits: