We're looking for a Site Start-Up Specialist, working in the Pharmaceuticals & Medical Products industry in Irvine, California, United States.
Executes study start-up for assigned protocols with the goal of meeting study start-up timelines.
Monitors project plans to meet Site Initiation Readiness at the Investigator Meeting.
Ensures the accuracy and quality of deliverables from clinical team and vendors.
Maintains project metrics and provide status updates to senior management.
We are offering Competitive Compensation and Benefits. This position may present an opportunity to go permanent.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
Bachelors degree in Life Sciences or related field
2 years experience in clinical research
IRB submission and regulatory documentation experience
Prior experience as Study Start-Up Specialist but not mandatory
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.