BACK TO JOBS

Senior Clinical Research Associate (West Coast) – Leading Biopharma Organization

APPLY NOW
Title: Senior Clinical Research Associate- Leading Biopharma Organization
Position Type: Permanent
Specialty Therapeutic Areas: Oncology, immunology, antiviral, CNS, inflammation, autoimmune disorders, endocrinology, cardiovascular, respiratory, ophthalmology, rare orphan diseases and gene therapies.
Location: San Francisco, CA
Compensation: up to $130k
Travel Requirements: 50%

Brio Resource Group is a search firm committed to providing rare pharmaceutical talent on an executive search basis to the Pharmaceutical, Biopharma, Device and CRO industries. We work on behalf of organizations that value true talent acquisition partners and specialize in supporting emerging companies. Our many years of experience, subject matter expertise, proven search process and genuine passion to deliver rare talent defines Brio.

We work with organizations across several industry disciplines, with our strongest portfolio in Drug Development and Clinical Research. With US offices located in Washington DC (East Coast) and San Diego (West Coast) we connect rare talent with emerging companies nationwide.

Job Description:

We are recruiting for critical permanent positions on behalf of a leading biopharmaceutical services company to add talented Senior Clinical Research Associates to their team. The Senior CRA would perform the clinical monitoring aspect of designated projects in accordance with study specific procedures, applicable SOPs, and regulations. Act as the company's direct contact with assigned clinical sites and use judgment to assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites. Performs site selection, initiation, monitoring and close out visits at investigator sites according to project schedule. Adheres to project guidelines and company SOPs for monitoring requirements.

Monitor activities at clinical study sites to assure adherence to GCP, ICH, SOPs and study protocols.

We welcome the opportunity to provide a full job description upon resume review.

Highlights & Requirements:

  • Education: (bachelors or greater in biological science, pharmacy, or other health-related discipline preferred)
  • Equivalent nursing qualification or other equivalent experience.
  • Greater than 3 years of clinical monitoring experience within a CRO or pharmaceutical company
  • Expertise in major multi-therapeutic areas such as oncology, immunology, antiviral, CNS, inflammation, autoimmune disorders, endocrinology, cardiovascular, respiratory, ophthalmology, rare orphan diseases and gene therapies.
  • Excellent written and communication skills

How To Apply:

Once you click “APPLY” an appropriate member of our executive recruitment team will review your credentials and respond to arrange an initial interview to review your credentials and career objectives.

We respond to applicants who meet our position requirements, but suggest submitting your resume for future consideration for our expanding list of new opportunities surfacing daily within our Biopharma network. We have a strict honor code at Brio respecting your confidentiality and we only share your information with your consent.

Brio Resource Group, LLC considers all applicants without regard to race, color, religion, sex, national origin, age, mental or physical disabilities, or any other similarly protected status.