PSG Global Solutions Careers
Clinical Operations Lead III
PSG Global Solutions Careers, Cambridge, Massachusetts, us, 02140
Apply now and our proprietary system will quickly have you in front of a live recruiter.The OpportunityDescriptionWe're looking for a
Clinical Operations Lead III , working in
Pharmaceuticals and Medical Products
industry in
250 Kendall Street, Cambridge, Massachusetts, 02142, United States .
Partners with Medical Research and other functions to develop operationally feasible and clear protocol concepts and final protocols.Leverage Phase and operational expertise to establish study level operational strategy in alignment with the Clinical Development Plan (CDP) and program level strategy.Independently oversees one or more trials by establishing the operational strategy and securing excellence in execution through the CRO partner.
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
At least 10 years of clinical research study management experience of which at least 4 years has been with a sponsor company managing outsourced clinical trials within quality, timeline, and budget expectations a plusPrior CRO or investigator site and/or monitoring experience is a plus
Deep understanding of clinical development within one or more Phases of trials (Phase I, II, III, IV) and a working understanding of cross functional drug developmentScientific learning agility to quickly develop a sound working knowledge of new therapeutic areasAbility to establish operational plans and support the CRO in the execution of the plansRequires a balance of scientific and operational/project management and team leadership expertiseMust be able to build effective relationships across and up and down the organizationExcellent project management skills, including risk assessment and contingency planningMust have effective prior CRO management skills and be able to adapt to the GCO outsourcing modelAble to partner with other functions and both internal and external stakeholders
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 Operations Lead III , working in
Pharmaceuticals and Medical Products
industry in
250 Kendall Street, Cambridge, Massachusetts, 02142, United States .
Partners with Medical Research and other functions to develop operationally feasible and clear protocol concepts and final protocols.Leverage Phase and operational expertise to establish study level operational strategy in alignment with the Clinical Development Plan (CDP) and program level strategy.Independently oversees one or more trials by establishing the operational strategy and securing excellence in execution through the CRO partner.
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
At least 10 years of clinical research study management experience of which at least 4 years has been with a sponsor company managing outsourced clinical trials within quality, timeline, and budget expectations a plusPrior CRO or investigator site and/or monitoring experience is a plus
Deep understanding of clinical development within one or more Phases of trials (Phase I, II, III, IV) and a working understanding of cross functional drug developmentScientific learning agility to quickly develop a sound working knowledge of new therapeutic areasAbility to establish operational plans and support the CRO in the execution of the plansRequires a balance of scientific and operational/project management and team leadership expertiseMust be able to build effective relationships across and up and down the organizationExcellent project management skills, including risk assessment and contingency planningMust have effective prior CRO management skills and be able to adapt to the GCO outsourcing modelAble to partner with other functions and both internal and external stakeholders
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?