R&D Partners
Senior Clinical Trial Specialist
R&D Partners, San Francisco, California, United States, 94199
Base pay range
$115,000.00/yr - $124,500.00/yr
R&D Partners is seeking to hire a Senior Clinical Trial Specialist in the San Francisco Bay Area.
This is a hybrid role requiring on‑site presence at least 2 days per week.
Responsibilities
Lead tasks related to the oversight of site monitoring, vendor management, and other activities.
Support study‑related matters that impact study participant safety, data integrity, study timelines, quality, and budget.
Oversight of CRO for IRB/EC related submission/approval activities.
Oversee site and investigator training materials.
Contribute to global study operations risk identification and mitigation.
Qualifications
BA/BS in Nursing, Life or Health sciences (preferred).
3–5 years of ClinOps experience within a biotech or pharmaceutical company.
Demonstrated experience with oversight of external vendors including SOW, budgets, purchase orders and invoice management.
Benefits
Medical insurance – PPO, HMO & HSA.
401k plan.
Employee Assistance Program.
Long‑term disability.
Weekly payroll.
Online timecard approval.
Competitive compensation: $115,000 to $124,500 (dependent on experience).
R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
R&D Partners is an equal‑opportunity employer.
Seniority level Associate
Employment type Full‑time
Job function Project Management
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R&D Partners is seeking to hire a Senior Clinical Trial Specialist in the San Francisco Bay Area.
This is a hybrid role requiring on‑site presence at least 2 days per week.
Responsibilities
Lead tasks related to the oversight of site monitoring, vendor management, and other activities.
Support study‑related matters that impact study participant safety, data integrity, study timelines, quality, and budget.
Oversight of CRO for IRB/EC related submission/approval activities.
Oversee site and investigator training materials.
Contribute to global study operations risk identification and mitigation.
Qualifications
BA/BS in Nursing, Life or Health sciences (preferred).
3–5 years of ClinOps experience within a biotech or pharmaceutical company.
Demonstrated experience with oversight of external vendors including SOW, budgets, purchase orders and invoice management.
Benefits
Medical insurance – PPO, HMO & HSA.
401k plan.
Employee Assistance Program.
Long‑term disability.
Weekly payroll.
Online timecard approval.
Competitive compensation: $115,000 to $124,500 (dependent on experience).
R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
R&D Partners is an equal‑opportunity employer.
Seniority level Associate
Employment type Full‑time
Job function Project Management
#J-18808-Ljbffr