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Clinical Research Associate Contract: Alameda, California, US
Salary Range: 45.00 - 50.00 | Per Hour
Job Code: 362806
End Date: 2025-07-10
Days Left: 2 days, 3 hours left
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To discuss more about this job opportunity, please reach out to Deepak Arya (LinkedIn URL - email your updated resume at Email - deepak.arya@collabera.com. Thank you! Pay rate: $45 - $50/hr. Industry: Medical Device
Job Description: - This position will include monitoring and oversight of clinical sites to ensure timely and successful execution of clinical studies, resolving study-related discrepancies.
- This position will ensure compliance with protocol and all regulatory policies, procedures, and/or guidelines during clinical studies by training/guidance of investigators/study coordinators, and follow-up of corrective actions.
- Also, will ensure validity of study by identifying/resolving discrepancies and obtaining missing data and may track more routine aspects of a study. of clinical documents, which may include protocols, case report forms (CRFs), memos, correspondence, reports, and other required documents. Also, conduct new CRA orientation, onboarding, and training activities.
- Candidate will proactively identify, and address issues related to study monitoring and clinical site management.
- Track and communicate monitoring and site management updates and issues; escalate monitoring-related study timeline and quality risks to the Clinical leadership.
- Maintain clinical operations processes, new employee onboarding, internal protocol training, monitoring tracking tools and study tools/templates for CRAs and site personnel.
- Manage CROs/vendors for outsourced activities as applicable, including sponsor oversight of relevant functional activities (e.g., study management, monitoring, site management, project master files, and data management).
- Ensure adherence to Good Clinical Practices, Industry standards, standard operating procedures and to all other regulatory and quality standards in conducting Lingo Clinical research and development.
- Operate under minimal supervision and demonstrate a high degree of proficiency.
- Undertake additional projects and tasks as determined by department and organizational needs.
- The successful candidate will demonstrate the ability to work collaboratively across
cross-functional teams, including Quality, Compliance, Product Development, and Engineering, etc. - They should have prior experience in Clinical Research or Clinical Trials and a solid understanding of related processes.
- This role requires someone who is a quick thinker, adaptable to evolving workflows, and proactive in seeking clarification when needed.
- This role requires a resourceful and agile individual who can think critically, adapt to evolving workflows, and proactively seek clarification when needed. The ideal candidate will also demonstrate creativity in problem-solving and be open to exploring innovative ideas and process improvements.
- The ideal candidate must be able to quickly learn internal processes and demonstrate the ability to work independently with minimal supervision.
- While support is always available, this role requires someone who can take initiative and adapt quickly in a fast-paced environment.
Education: - Bachelor's degree-Major/Field of Study- Biology, Health Sciences, Computer Science, or equivalent
- Licenses and Certifications
Job Requirement - Clinical Study Monitoring
- Clinical Document Management
- Protocol Adherence
- Regulatory Policies
- Project Master Files
Reach Out to a Recruiter - Recruiter
- Email
- Phone
- Deepak Arya
- deepak.arya@collabera.com
Apply Now Collabera
Job Tags
Hourly pay, Contract work,