Clinical Research Associate
Clinical Research Associate
Proven Recruiting
San Diego, CA
See who Proven Recruiting has hired for this role
Clinical Research Associate (Fully onsite in San Diego) – Contract to Hire
If culture and mentorship are your priorities – you’ve found your match. This pioneer company in Oncology studies is looking to support and promote a talented CRA who will assist with the clinical operations andsite monitoring according to GCPs. The ideal professional will have a strong background with site monitoring and knowledge of clinical operations and regulatory requirements.
What you will do:
Note: We actively support and promote people of various backgrounds, from race, religion, gender to geographical area, university, lifestyle, and personality type. Proven Recruiting is minority-owned, majority women, and is a strong advocate for diversity and inclusion in the broader community. Apply today!
If culture and mentorship are your priorities – you’ve found your match. This pioneer company in Oncology studies is looking to support and promote a talented CRA who will assist with the clinical operations andsite monitoring according to GCPs. The ideal professional will have a strong background with site monitoring and knowledge of clinical operations and regulatory requirements.
What you will do:
- Conducts pre-study (site qualification) and routine monitoring to ensure visits are completed according to the Clinical Monitoring Plan(s) and SOPs.
- Trains the study investigators
- Prepares site visit reports and verifies data entered into the case report forms (CRFs) is consistent with subject clinical records, electronic medical records and source data to ensure accuracy
- Ensures data collection timelines and deliverables are met at assigned clinical sites in accordance with study plans
- Bachelor’s Degree (BA/BS) in life sciences and minimum of three or more years of relevant experience in clinical research or healthcare related industry, including a minimum of 2 years direct field monitoring experience, or equivalent combination of education and experience
- Experience working at a Sponsor and performing Independent site monitoring in ideally all phases, but Phase I is required.
- Experience in oncology is highly preferred
- Experience/training in the following areas: GCP Regulations, ICH Guidelines, 21CFR, HIPAA, Drug Development and Approval Process
- Compensation is determined by several factors which may include skillset, experience level, and geographic location. The expected range for this role is $80k – $120k per year. Please note this range is an estimate and actual pay may vary based on qualifications and experience.
Note: We actively support and promote people of various backgrounds, from race, religion, gender to geographical area, university, lifestyle, and personality type. Proven Recruiting is minority-owned, majority women, and is a strong advocate for diversity and inclusion in the broader community. Apply today!
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Seniority level
Associate -
Employment type
Contract -
Job function
Research, Analyst, and Information Technology -
Industries
Staffing and Recruiting
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