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Director Clinical Development Jobs in Minnesota (NOW HIRING)

DaVita

$77K - $105K/yr

The Sr. Director, Clinical Services & Operations is responsible for setting the clinical strategy ... Create space for regular development conversations and advocate for TM growth opportunities ...

DaVita

... America Director, Clinical Services - Hospital Programs The Director, Clinical Services (DCS ... Clinical Leadership & Talent Development * Leads and coaches the Hospital Clinical Services ...

Childrens Health Care

Dir Mental Health

Saint Paul, MN · On-site

... clinical and administrative leadership and expertise. The director facilitates an atmosphere of inclusive, situational management and the development of collegial relationships among department ...

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Director Clinical Development information

See Minnesota salary details

$49K

$124K

$207.6K

How much do director clinical development jobs pay per year?

As of Aug 5, 2026, the average yearly pay for director clinical development in Minnesota is $124,032.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,600.00 and $148,400.00 per year, depending on experience, location, and employer.

What does a director of clinical development do?

A Director of Clinical Development oversees the planning, execution, and management of clinical trials to ensure the safety and efficacy of new therapies. They collaborate with cross-functional teams, regulatory agencies, and key stakeholders to design and implement clinical strategies. Their role includes protocol development, trial monitoring, and ensuring compliance with regulatory standards. Additionally, they analyze trial data, manage budgets, and contribute to the overall drug development process.

What are the most common challenges faced by a director of clinical development?

Directors of Clinical Development often navigate challenges such as aligning multiple cross-functional teams, managing complex project timelines, and ensuring compliance with evolving regulatory standards globally. They may also need to address issues related to trial participant recruitment, data integrity, and budget management. Adapting quickly to shifting priorities while maintaining high ethical and scientific standards is crucial. Successful Directors leverage collaboration, proactive problem-solving, and their in-depth industry knowledge to overcome these challenges and deliver impactful clinical results.

What are the key skills and qualifications needed to thrive as a director of clinical development?

A Director Clinical Development typically requires an advanced degree in life sciences or medicine, extensive experience in clinical research, and a strong understanding of regulatory guidelines. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are highly valued. Exceptional leadership, strategic thinking, and effective cross-functional communication set outstanding candidates apart. These competencies ensure clinical programs are executed efficiently, ethically, and in alignment with organizational goals.

What are the most commonly searched types of Clinical Development jobs in Minnesota? The most popular types of Clinical Development jobs in Minnesota are:
What are popular job titles related to Director Clinical Development jobs in Minnesota? For Director Clinical Development jobs in Minnesota, the most frequently searched job titles are:
What job categories do people searching Director Clinical Development jobs in Minnesota look for? The top searched job categories for Director Clinical Development jobs in Minnesota are:
Director Clinical Development jobs near you
Infographic showing various Director Clinical Development job openings in Minnesota as of July 2026, with employment types broken down into 100% Full Time. Highlights an 60% In-person, and 40% Remote job distribution, with an average salary of $124,032 per year, or $59.6 per hour.

Clinical Development Scientist

ComTec Information Systems

Plymouth, MN • On-site

Contractor

Re-posted 26 days ago

Job description

Job Title - Clinical Development Scientist;
Hybrid role. 3 days/week in office
Bothell WA/Cambridge MA/ Plymouth MN

12 Months


Ultrasound, Senior Clinical Development Scientist The Senior Clinical Development Scientist for the Ultrasound group will be responsible for developing, generating, and disseminating clinical and economic evidence ensuring innovation, and transformation with best-in-class clinical evidence. Your role: Contribute strategic guidance for clinical and economic evidence related to the end to end (E2E) development process from ideation through post-market for products in the Ultrasound business. Collaborate with key internal and external stakeholders to provide in-depth expertise to develop and lead clinical initiatives through non-clinical and clinical strategies for new product development initiatives and product life cycle management. Drive execution ensuring quality and timeliness of clinical programs and/or trials to support critical regulatory requirements, be agile and responsive during course of design, execution, and interpretation of trial data. Collaborate with investigators, IRBs/ECs, Regulatory Agencies, societies, and associations; and additionally, to support claims, reimbursement, health economic outcomes and/or market access. Ensure appropriate preparation, interpretation and dissemination of all evidence generated, including Clinical Study Reports (CSRs), Clinical Evaluation Reports (CERs), abstracts, peer-reviewed manuscripts, as assigned. Lead or support scientific discussions with regulatory agencies or notified bodies, including proposed clinical investigations; review process of clinical evidence generated for marketing authorization, in line extensions, including during sponsor regulatory inspections.

You are the right fit if:

You have acquired 7+ years of experience in clinical research/development/real world evidence (RWE); scientific study design, strong scientific background and experience with Artificial Intelligence algorithm clinical performance validation. You have deep expertise including innovative clinical trial design, registries, quality improvement initiatives, and creation of data networks and working knowledge of biostatistics. Your skills include a demonstrated working knowledge of GCP, FDA regulations and EU-MDR regulations, and in-depth understanding of product development and associated design controls for medical devices. You have strong writing skills to product quality clinical documents, including final reports. Strong knowledge and experience with study design is also desired. You have an ability to write original scientific documentation such as clinical study reports, regulatory filings, investigator brochures, clinical evaluation reports, internal reports and scientific publications. You have a medical or scientific education (MD or PhD). You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this Clinical position. You are self-directed with a strong work ethic, agile, and have an ability to work in a purposeful environment. You can collaborate effectively and influence decision making with various teams cross-functionally, as well as externally. You can think analytically, present statistical methods and results to a variety of audiences, especially non-statisticians. You can travel up to 15% (domestic and international) according to business needs.,