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Clinical Study Design Manager Jobs (NOW HIRING)

Science 37

Clinical Study Design Manager

Boston, MA · On-site

$150 - $200/hr

The Clinical Study Design Manager is responsible for working with our clients and internal staff to define the eSource platform specification design for the study, including all data capture ...

Science 37

Clinical Study Design Manager

Boston, MA · On-site

The Clinical Study Design Manager is responsible for working with our clients and internal staff to define the eSource platform specification design for the study, including all data capture ...

Science 37

Clinical Study Design Manager

Raleigh, NC · On-site

$125 - $150/hr

The Clinical Study Design Manager is responsible for working with our clients and internal staff to define the eSource platform specification design for the study, including all data capture ...

Doist

Clinical Study Design Manager

Morrisville, NC · On-site

$125 - $150/hr

The Clinical Study Design Manager is responsible for working with our clients and internal staff to define the eSource platform specification design for the study, including all data capture ...

Science 37

$125 - $150/hr

The Clinical Study Design Manager is responsible for working with our clients and internal staff to define the eSource platform specification design for the study, including all data capture ...

Science 37

$150 - $200/hr

The Clinical Study Design Manager is responsible for working with our clients and internal staff to define the eSource platform specification design for the study, including all data capture ...

RQMIS Inc

Be Seen First

Clinical Trials Project Manager

Amesbury, MA · On-site

RQMIS Inc. is a fast growing, medical device/biotechnology consultancy with a focus on regulatory strategy/submissions, clinical study design/management and quality systems design/compliance/auditing.

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site

This Lead Clinical Study Manager-4 (CSM IV) / Senior Clinical Study Manager role will develop and ... Partner with internal stakeholders, investigators and KOLs to develop and review study design and ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

This Lead Clinical Study Manager-4 (CSM IV) / Senior Clinical Study Manager role will develop and ... Partner with internal stakeholders, investigators and KOLs to develop and review study design and ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

The Senior (Clinical Study Manager 4) role will develop and execute strategies for clinical and ... Collaborate with internal stakeholders, investigators and KOLs to develop and review study design ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

The Senior (Clinical Study Manager 4) role will develop and execute strategies for clinical and ... Collaborate with internal stakeholders, investigators and KOLs to develop and review study design ...

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Clinical Study Design Manager information

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$22K

$125.3K

$206K

How much do clinical study design manager jobs pay per year?

As of Sep 9, 2026, the average yearly pay for clinical study design manager in the United States is $125,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $157,000.00 per year, depending on experience, location, and employer.

What does a clinical study design manager do?

A Clinical Study Design Manager is responsible for planning and overseeing the design of clinical trials to ensure they are scientifically sound, ethical, and compliant with regulatory standards. They collaborate with cross-functional teams to develop study protocols, determine study objectives, and select appropriate methodologies. Their role also includes managing timelines, budgets, and ensuring the quality of data collected. Ultimately, they play a crucial part in advancing medical research by ensuring studies are set up for success.

What are the key skills and qualifications needed to thrive as a clinical study design manager?

To thrive as a Clinical Study Design Manager, you need a strong background in life sciences, experience in clinical research, and often an advanced degree such as an MS, MPH, or PhD. Familiarity with clinical trial management systems (CTMS), statistical analysis software, and knowledge of regulatory guidelines like GCP and ICH are typically required. Excellent project management, leadership, and cross-functional communication skills distinguish top performers in this role. These competencies ensure the efficient design, execution, and oversight of clinical studies that meet regulatory standards and scientific objectives.

What are some common challenges faced by clinical study design managers when coordinating cross-functional teams during the planning phase of a clinical trial?

Clinical Study Design Managers often encounter challenges in aligning the priorities and timelines of cross-functional teams, such as clinical operations, biostatistics, regulatory affairs, and medical writing. Ensuring clear communication and maintaining a cohesive strategy across these diverse groups is essential to prevent delays and ensure protocol feasibility. Additionally, balancing scientific integrity with regulatory requirements and operational constraints requires proactive problem-solving and strong negotiation skills. Successful managers foster collaboration by facilitating regular meetings, leveraging project management tools, and encouraging open dialogue among stakeholders.

What is the difference between Clinical Study Design Manager vs Clinical Research Associate?

AspectClinical Study Design ManagerClinical Research Associate
CredentialsTypically requires a master's degree in life sciences or related field; relevant certifications like CCRP or SOCRA are commonOften holds a bachelor's degree in life sciences; certifications like CCRP or RAC are advantageous
Work EnvironmentLeads study design, planning, and protocol development; works closely with cross-functional teamsMonitors clinical trials at sites; ensures compliance and data integrity
Industry UsageUsed in planning and overseeing clinical studies from inception to completionPrimarily involved in site monitoring and data collection during trials

The Clinical Study Design Manager focuses on designing and planning clinical studies, ensuring protocols meet scientific and regulatory standards. In contrast, the Clinical Research Associate is more involved in monitoring ongoing trials at clinical sites to ensure compliance and data quality. Both roles are essential in the clinical research process but differ in scope and responsibilities.

What are popular job titles related to Clinical Study Design Manager jobs?

For Clinical Study Design Manager jobs, the most frequently searched job titles are:

Infographic showing various Clinical Study Design Manager job openings in the United States as of July 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $125,290 per year, or $60.2 per hour.

Clinical Study Design Manager

Morrisville, NC • On-site

Science 37
Scientific Research and Development Services • 501 - 1,000 employees
Learn more about Science 37external

Full-time

Posted 29 days ago

Job description

POSITION OVERVIEW
Science 37 accelerates clinical research by expanding patient access to trials, leading to faster approvals and better health outcomes for all. Our solutions empower life sciences companies to reach diverse populations beyond traditional means of conducting clinical research.
The Clinical Study Design Manager is responsible for working with our clients and internal staff to define the eSource platform specification design for the study, including all data capture requirements, bridging the gap between protocol requirements and implementation. This role oversees the comprehensive lifecycle of the eSource platform, from initial design and specification to final build and implementation. A critical component of this position is the oversight of offshore build teams, ensuring all design and build requirements remain on track and meet the highest standards of quality and efficiency.
DUTIES AND RESPONSIBILITIES
Duties include but are not limited to:
  • Define and specify eSource design requirements for assigned studies, collaborating closely with internal teams and clients to ensure protocol alignment.
  • Work with offshore teams to ensure all platform design and build milestones are met according to project timelines and technical specifications.
  • Serve as the SME for system capabilities, data capture configuration, and the validation of the eSource Platform.
  • Drive efficiency by implementing standard templates and libraries and contributing to the development of streamlined building and QC
  • Collaborate in highly cross-functional project teams, interacting with Clients, Site Operations Managers, and internal staff to document data collection requirements.
  • Create and maintain project timelines, monitoring progress of all design activities while remaining accountable for quality metrics, KPIs, and performance benchmarks.
  • Lead the build, testing, and implementation of direct data capture services, ensuring system integration and user acceptance testing to meet quality deliverables.
  • Participate in the review and revision of SOPs and work instructions.
  • Train and mentor Platform Build Managers and support specialists to foster a culture of excellence and operational speed.
  • Oversee and perform user access management for all Science 37 eSource platforms.
  • Partner with Clinical Operations and Data Management to provide early strategic input on protocol design and execute post-production changes.
  • Build and maintain effective working relationships with clients, sponsors, and vendors to ensure project success.

QUALIFICATIONS & SKILLS
Qualifications
The following qualifications are preferred and/or equivalent applicable experience:
  1. Required: 3+ years of experience in clinical research or life science industry, including at least 3 years in design of CRF/ePRO or other clinical trials database capture software.
  2. Required: 2+ years of CRIO platform experience is required.
  3. Bachelor's degree or equivalent experience in the health science field.
  4. Extensive knowledge of the clinical research development process
  5. Experience in a fast-moving, growth-minded company, and are comfortable with needing to be flexible and adaptable as requirements change.

Skills/Competencies
  1. Understanding of drug development process and regulatory guidelines.
  2. Knowledgeable about the critical elements for success in clinical trials; participation in and contribution to these activities
  3. Ability to create and review protocols, programs, and assess the success of a project.
  4. Experience in building and guiding organizational teams, leveraging each team member's unique background and perspective to achieve team goals while providing clear direction and accountabilities
  5. Proactive problem-solving abilities and follow through
  6. Successful situational responsive decision-making
  7. Strong communication and presentation skills - both written and verbal
  8. Ability to articulate ideas to both technical and non-technical audiences
  9. Ability to establish and maintain positive sponsor, project team member, vendor and internal Science37 relationships
  10. Have excellent time management skills, action-oriented, goal-oriented, and innovative 11. Demonstrates high level of attention to detail, outstanding organizational activities and good blend of analytical skills, strategic thinking, planning and implementation
  11. Working knowledge of Microsoft Office suite, Google applications, and electronic clinical technologies.
  12. Demonstrated ability to foster concepts of teamwork, cooperation, self- control, and flexibility to get the work done

REPORTING
The reporting leader will assign projects, provide general direction and guidance. The incumbent is expected to perform duties and responsibilities with minimal supervision.
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