Join Freenome as a Contract Clinical Research Associate to impact cancer diagnostics through clinical trial management.
Posted by employer 6 months ago
First seen on Joblaze 1 week ago
Last verified on the company career page 1 day ago
Skills & Technologies
Requirements
- Experience
- 3+ years
- Education
- Bachelor's degree
Not disclosed in this posting: compensation, visa sponsorship.
Joblaze summary
The Contract Clinical Research Associate at Freenome plays a crucial role in managing clinical trial monitoring and site management, ensuring compliance with protocols and regulatory standards. This position requires a strong background in clinical trials, particularly in diagnostics, along with proficiency in tools like Veeva Vault and Medrio. Ideal candidates will have at least three years of relevant experience and a degree in a life science field, making this role suitable for mid-level professionals looking to impact cancer research. Freenome emphasizes a collaborative environment dedicated to advancing cancer detection.
Joblaze insights
- Listed 9 days ago on Joblaze — tracked directly from Freenome's career page.
- Freenome has 28 other open roles including Technical Product Manager III, Senior Bioinformatics Research Engineer, Senior Software Engineer II.
- 2 active Good Clinical Practice roles on Joblaze right now.
Quick facts
- Is the Clinical Research Associate (Contractor) role remote?
- Yes — Freenome lists this as a fully remote position.
- How much experience is required?
- At least 3 years of relevant experience for this Clinical Research Associate (Contractor) role.
- What's the tech stack?
- Joblaze extracted these technologies from the posting: Good Clinical Practice, Medrio, Veeva Vault.
- What seniority level is this role?
- Freenome targets mid-level candidates for this position.
- Is this full-time or contract?
- Contract for this Clinical Research Associate (Contractor) role at Freenome.
From the original posting
About this opportunity:
At Freenome, we are seeking a Contract Clinical Research Associate to help grow the Freenome Clinical Development team. The ideal candidate is well-organized, an excellent communicator and experienced in diagnostics clinical trial management. This person is responsible for all things related to assigned aspects of clinical trial monitoring and site management. You are passionate about clinical research, attention to detail and Good Clinical Practice, and you will have a significant impact on the continued growth of an organization dedicated to changing the entire landscape of cancer.
The role reports to the Director of Clinical Operations, Dennis McHugh. This role will be a Remote role with occasional travel, as required, to our Brisbane, California headquarters.
What you’ll do:
- Ensure compliance with standard protocol and regulatory and ICH GCP obligations in assigned aspects of clinical site monitoring, such as site initiation, routine monitoring, maintenance of study files, study close out, and retrieval of study materials.
- Complete on-site and remote monitoring activities in compliance with the Clinical Monitoring Plan, including source document verification for accuracy and integrity, as required.
- Write and submit reports of investigational site findings and update applicable tracking systems, as required; escalate observed deficiencies and issues as appropriate.
Must haves:
- Minimum Bachelor’s degree in a life science-related field, a registered nurse (RN) certification, or equivalent.
- 3+ years’ experience in a clinical trials research environment required, with specific in vitro diagnostics study experience.
- General knowledge of regulatory requirements & GCP.
- Ability to multi-task, deal with shifting priorities, and proactively solve problems/manage risks.
- Strong interpersonal, collaborative, and time management abilities.
- Excellent organizational skills; accurate and detail-oriented.
- High proficiency in Veeva Vault and Medrio.
- Strong spoken and written communication skills.
Nice to haves:
- CRA certification by recognized professional organization is a plus, but not mandatory.
- Previous experience in the cancer early detection space.
Additional information:
Contractors may be hired through a third-party provider and will be considered contingent workers. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information.
Freenome is proud to be an equal opportunity employer and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.
Applicants have rights under Federal Employment Laws.
- Family & Medical Leave Act (FMLA)
- Equal Employment Opportunity (EEO)
- Employee Polygraph Protection Act (EPPA)
California applicants please review the CCPA Notice at Collection here:
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