Sr Clinical Technical Project Manager

Meet the team: 

The Senior Clinical Technical Project Manager provide leadership and direction to Clinical Affairs in planning and execution of clinical strategies in a key business area. A successful leader in this role will understand and translate business strategy into planning an execution of clinical studies to support broader objectives.  

Excellent communication skills are required to manage and facilitate collaborations within the Clinical Affairs team, with all internal core team functional groups, and with external partner stakeholders. This role requires a strong technical background and experience in both product development and clinical study planning and execution, ideally in a regulated environment such as medical device development. 

Where you come in:  

• You will serve as a member of core team(s), providing strategic direction to study teams to meet goals and timelines  

• You will interface with representatives from key functional groups including Executive Management, Product Development/R&D, Regulatory Affairs, Quality Assurance, and Operations as well as Clinical Research Organizations (CROs) to set operational direction and strategy for clinical study activities. 

• You will work in collaboration with functional leaders to design/implement strategies and track project plans related to study design 

• You will drive the full spectrum of the clinical execution from the design phase to close-out in collaborating closely with the study team.   

• You will track and manage strategic study operations including KPIs, study timelines, all budgetary and financial information, etc. 

• You will coordinate and prioritize activities amongst trials/establish study milestones to ensure timelines are met 

• You will recommend and implement innovative ideas to increase efficiency and quality of study management activities 

• You will identify and mitigate risks to study implementation, enrollment, conduct, compliance, and completion  

• You will drive selection of Contract Research Organizations (CROs) through competitive bid process and other necessary vendors to support study requirements  

• You will provide oversight and execution of CRO study deliverables to ensure that objectives are met 

What makes you successful:  

• Bachelor’s degree in biological sciences or related medical/scientific field with a minimum X years leading clinical studies   

• You have a strong regulatory knowledge, including Good Clinical Practices (GCPs). 

• You have experience with protocol and ICF development. 

• You have experience with clinical study planning and execution in the medical device industry. 

• You have exceptional organizational skills and ability to deal with competing priorities, also strong reasoning and problem-solving ability. 

• You have excellent communication (written and verbal) and presentation skills along with leadership qualities. 

• You have strong interpersonal skills and ability to work effectively on cross-functional & global teams. 

• You thrive in an extremely fast-paced environment. 

Optional/nice to have: 

• Successful experience managing outside CRO groups in Class II/III, preferably diabetes, device studies 

• Proficient with MS Office Suite (Excel, Word and PowerPoint), MS Project, and Smartsheet 

What you’ll get:  

• A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community. 

• A full and comprehensive benefits program. 

• Growth opportunities on a global scale. 

• Access to career development through in-house learning programs and/or qualified tuition reimbursement. 

• An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities we serve.  

Travel Required:  

• 5-15% 

Experience and Education Requirements:  

• Typically requires a Bachelor’s degree in a technical discipline, and a minimum of 2-5 years related experience or Master’s degree and 0-2 years’ equivalent experience. 

Remote Workplace: Your location will be a home office; you are not required to live within commuting distance of your assigned Dexcom site (typically 75 miles/120km). If you reside within commuting distance of a Dexcom site (typically 75 miles/120km) a hybrid working environment may be available. Ask about our Flex workplace option.