Clinical Program Manager

DexCom Lithuania, UAB

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Clinical Program Manager

The Company

Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom began as a small company with a big dream: To forever change how diabetes is managed. To unlock information and insights that drive better health outcomes. Here we are 25 years later, having pioneered an industry. And we're just getting started. We are broadening our vision beyond diabetes to empower people to take control of health. That means personalized, actionable insights aimed at solving important health challenges. To continue what we've started: Improving human health.

We are driven by thousands of ambitious, passionate people worldwide who are willing to fight like warriors to earn the trust of our customers by listening, serving with integrity, thinking big, and being dependable. We've already changed millions of lives and we're ready to change millions more. Our future ambition is to become a leading consumer health technology company while continuing to develop solutions for serious health conditions. We'll get there by constantly reinventing unique biosensing-technology experiences. Though we've come a long way from our small company days, our dreams are bigger than ever. The opportunity to improve health on a global scale stands before us.

Meet The Team:

As a Clinical Program Manager you will 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:

Education & years of experience requirements auto-populate in the req no need to add them here!
Bachelors degree in biological sciences or related medical/scientific field with a minimum 5-8 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.
Successful experience managing outside CRO groups in Class II/III, preferably diabetes, device studies would be an advantage
Proficient with MS Office Suite (Excel, Word and PowerPoint), MS Project, and Smartsheet would be an advantage

What You'll Get:

A comprehensive onboarding and training on the job
Opportunity to work in a diverse and inclusive environment with colleagues representing 45 different nationalities
Hybrid working model, offering the flexibility to work both remotely and in a modern, well-equipped office space
5 additional vacation days, with potential for more for parents, students, and other cases with approval
Opportunity to work from other countries for up to 30 days per year
Health Insurance including reduced premiums available for dependents
Life and Accident insurance coverage
3rd Pillar Private Pension plan
Health and Wellness programs, including access to online coaching and therapy sessions
Fertility, Family forming, Menopause and Mens health support services
Regular team-building events that foster collaboration and connection
Best-in-class training and career development programs
Exclusive discounts on restaurants, spas, clothing, gyms, entertainment, and more
Access to a fitness tracking app with rewards for staying active
Free parking space at the city center office location.

Travel:

0-5%

Experience and Education Requirements:

Typically requires a Bachelors degree in a technical discipline, and a minimum of 8-12 years related experience or Masters degree and5-7 years equivalent industry experience or a PhD and 2-4 years of experience.

To all Staffing and Recruiting Agencies: Our Careers Site is only for individuals seeking a job at Dexcom. Only authorized staffing and recruiting agencies may use this site or to submit profiles, applications or resumes on specific requisitions. Dexcom does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to the Talent Acquisition team, Dexcom employees or any other company location. Dexcom is not responsible for any fees related to unsolicited resumes/applications.

Monthly base salary for this position is from €4,363.33 to €5,390.00 gross. Final offer will depend on your qualifications, competencies, and professional experience.

Mėnesinis bruto atlyginimasBruto/mėn. € 4364 - 5390

Papildoma informacija: Final offer will depend on your qualifications, competencies, and professional experience.

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Kontaktinis asmuo
Jurgita Stikliūnė

Founded in 1999, Dexcom empowers people to take control of their diabetes through innovative continuous glucose monitoring systems. By listening to the needs of users, caregivers and healthcare providers, Dexcom simplifies and improves diabetes management around the world. Headquartered in San Diego, California, with additional offices in the U.S., Europe, and Asia Pacific.

Vilnius Global Business Services centre supports Dexcom operations and its customers across the EMEA region and will expand the company's patient support, customer advocacy, finance and accounting operations in Europe.