PSG Global Solutions Careers
Clinical Trial Lead
PSG Global Solutions Careers, Princeton Junction, New Jersey, us, 08550
Apply now and our proprietary system will quickly have you in front of a live recruiter.The OpportunityDescriptionWe're looking for a
Clinical Trial Lead , working in
Pharmaceuticals and Medical Products
industry in
Princeton Junction, New Jersey, United States .
Responsibilities:Overseeing a CRO team for assigned domestic and global protocols to ensure proper conduct and timely completion of projects.Contributing to the development and implementation of study strategy.Contributing to the development of protocol outlines, protocols, amendments, and Case Report Forms.
Our Client
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
Requirements:
Bachelor's degreeMinimum of 5 years experience in the pharmaceutical industryAt least 3 years' experience in leading multidisciplinary study teams from final protocol to database lock
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?
Clinical Trial Lead , working in
Pharmaceuticals and Medical Products
industry in
Princeton Junction, New Jersey, United States .
Responsibilities:Overseeing a CRO team for assigned domestic and global protocols to ensure proper conduct and timely completion of projects.Contributing to the development and implementation of study strategy.Contributing to the development of protocol outlines, protocols, amendments, and Case Report Forms.
Our Client
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
Requirements:
Bachelor's degreeMinimum of 5 years experience in the pharmaceutical industryAt least 3 years' experience in leading multidisciplinary study teams from final protocol to database lock
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?