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Clinical Research Associate

1-3 years
Not Disclosed
10 June 19, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Summary:

Join a leading life sciences company as a Clinical Research Associate (CRA) in Alameda, California. This on-site, contract role offers an excellent opportunity for professionals experienced in clinical trials, site monitoring, and vendor oversight. Contribute to high-quality clinical operations while ensuring regulatory compliance and Good Clinical Practice (GCP) standards.


Key Responsibilities:

  • Identify and address study monitoring and site management issues proactively.

  • Track, report, and escalate site performance risks to clinical leadership.

  • Support onboarding, protocol training, and documentation maintenance.

  • Oversee CROs and vendors in study operations, data management, and site activities.

  • Ensure strict compliance with GCP, SOPs, and regulatory guidelines.

  • Independently manage multiple priorities and dynamic tasks.

  • Contribute to departmental projects and improvement initiatives.


Required Skills & Qualifications:

  • Bachelor's degree in Biology, Health Sciences, Mathematics, Computer Science, or related field.

  • Prior experience in clinical research or clinical trials is mandatory.

  • Solid knowledge of clinical trial processes, monitoring standards, and regulatory protocols.

  • Strong organizational and problem-solving abilities.

  • Excellent communication skills for cross-functional teamwork.

  • Ability to manage workload independently with minimal supervision.


Perks & Benefits:

  • Competitive compensation: Up to $90,000 per year

  • Opportunity for contract extension beyond 6 months

  • Work in a dynamic and innovative clinical research environment

  • Collaborative cross-functional teams

  • Gain valuable experience managing CROs and clinical operations


Company Description:

GForce Life Sciences is a trusted partner in providing life sciences and healthcare staffing solutions across the US. Our client-focused approach connects talented clinical professionals with leading organizations, driving innovation in clinical development and patient care.


Work Mode:

On-site – Alameda, CA (5 days per week)


Call-to-Action:

Ready to advance your clinical research career? Apply now to join a team making an impact in clinical trial management and life sciences innovation.