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Clinical Development Manager Jobs in Bridgewater, MA

AstraZeneca

Clinical Development Scientist

Boston, MA · On-site

$203K - $305K/yr

Deviation Management: Investigate protocol deviations, identify root causes, and implement ... Clinical Development Planning: Support the design and execution of key elements of the Clinical ...

AstraZeneca

Clinical Development Scientist

Boston, MA · On-site

$203K - $305K/yr

Deviation Management: Investigate protocol deviations, identify root causes, and implement ... Clinical Development Planning: Support the design and execution of key elements of the Clinical ...

AstraZeneca

Clinical Development Scientist

Boston, MA · On-site

$203K - $305K/yr

Deviation Management: Investigate protocol deviations, identify root causes, and implement ... Clinical Development Planning: Support the design and execution of key elements of the Clinical ...

Astrazeneca

Clinical Development Scientist

Boston, MA · On-site

$203K - $305K/yr

Deviation Management: Investigate protocol deviations, identify root causes, and implement ... Clinical Development Planning: Support the design and execution of key elements of the Clinical ...

Avalyn Pharma

Director, Clinical Development

Boston, MA · On-site

The Director, Clinical Development works cross-functionally with Clinical Operations, Biostatistics, Regulatory Affairs, Pharmacovigilance, Translational Science, Data Management, and external CROs ...

Every Cure

Head of Clinical Development

Boston, MA · On-site

$86K - $118K/yr

The Head of Clinical Development leads Every Cure's clinical research and development function ... They manage a diverse portfolio of drug repurposing initiatives including Every Cure-sponsored ...

Every Cure

Head of Clinical Development

Boston, MA · On-site

$86K - $118K/yr

The Head of Clinical Development leads Every Cure's clinical research and development function ... They manage a diverse portfolio of drug repurposing initiatives including Every Cure-sponsored ...

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Clinical Development Manager information

What are the key skills and qualifications needed to thrive as a Clinical Development Manager?

To thrive as a Clinical Development Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a life sciences degree and relevant industry experience. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are commonly required. Strong leadership, problem-solving, and communication skills distinguish top performers in this role. These skills are vital for ensuring successful clinical trials, regulatory approval, and effective cross-functional collaboration.

How does a Clinical Development Manager typically collaborate with cross-functional teams during a clinical trial?

A Clinical Development Manager works closely with various cross-functional teams, including clinical operations, regulatory affairs, data management, and biostatistics, to ensure the successful execution of clinical trials. They facilitate communication between these departments, align project timelines, and address any operational challenges that arise. By fostering collaboration, they help ensure that studies are conducted in compliance with regulatory standards, data is accurately collected and analyzed, and that project milestones are met on schedule.

What is the difference between Clinical Development Manager vs Clinical Research Associate?

AspectClinical Development ManagerClinical Research Associate
Required CredentialsBachelor's or higher in life sciences, often with project management certificationsBachelor's in life sciences or related field, often with clinical research certifications
Work EnvironmentOversees multiple clinical trials, manages teams, and coordinates with stakeholdersMonitors clinical sites, ensures protocol compliance, and collects data
Employer & Industry UsagePharmaceutical companies, biotech firms, CROsResearch sites, CROs, pharmaceutical companies

The Clinical Development Manager focuses on overseeing the entire clinical development process, managing teams, and strategic planning. In contrast, the Clinical Research Associate primarily monitors clinical trial sites and ensures compliance. Both roles are essential in clinical research but differ in scope and responsibilities.

What does a clinical development manager do?

A clinical development manager oversees the planning, execution, and management of clinical trials to ensure they meet regulatory standards and project timelines. They coordinate with cross-functional teams, monitor trial progress, and ensure compliance with Good Clinical Practice (GCP) guidelines. Strong project management skills and knowledge of clinical research processes are essential for this role.

What cities near Bridgewater, MA are hiring for Clinical Development Manager jobs?

Cities near Bridgewater, MA with the most Clinical Development Manager job openings:

Clinical Development Manager jobs near you
Infographic showing various Clinical Development Manager job openings in Bridgewater, MA as of August 2026, with employment types broken down into 1% As Needed, 66% Full Time, 31% Part Time, and 2% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution.

Clinical Development Scientist

Boston, MA • On-site

AstraZeneca
Pharmaceutical Product Wholesalers • 10K+ employees

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

24th of 86 rated pharmaceutical

People enjoy working here

Good employer

Recommended by students

Learn more about AstraZenecaexternal

$203K - $305K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Job Title: Clinical Development Scientist
Location: Boston, MA or New Haven, CT
Introduction to role:
Are you ready to turn complex clinical data into confident decisions that accelerate life-changing medicines for people with severe, underserved conditions? As a Clinical Development Scientist based in Boston or New Haven, you will sit at the center of a cross-functional study team, strengthening study quality, safeguarding data integrity, and ensuring inspection readiness across critical programs.
You will connect protocol design, real-time data review, and operational execution-transforming signals into actions and actions into impact. From day one, you will help shape high-value trials, spotlight safety and efficacy trends early, and enable clear, timely decisions. Do you thrive at the intersection of science, operations, and data, guiding teams through complex questions with evidence and empathy?
Accountabilities:
  • Protocol and Study Document Leadership: Contribute to the development of clinical study protocols, operations manuals, charters, monitoring plans, and other essential documents that enable efficient, inspection-ready execution.
  • Safety and Efficacy Surveillance: Continuously monitor safety and efficacy data; escalate emerging concerns that warrant team awareness and intervention to protect participants and timelines.
  • Data Analytics for Quality: Use Medidata Rave, Elluminate, and related tools to detect gaps or inconsistencies across key datasets and drive corrective actions that improve data integrity.
  • Deviation Management: Investigate protocol deviations, identify root causes, and implement mitigations to prevent recurrence.
  • Stakeholder Engagement: Proactively collaborate with the internal study team, site staff, investigators, and CRO personnel to enable high-quality execution and consistent inspection readiness.
  • Trial Guidance and Issue Resolution: Serve as a point of contact for CRAs/CROs on protocol and trial procedure questions; manage and resolve issues that could impede study conduct.
  • Clinical Development Planning: Support the design and execution of key elements of the Clinical Development Plan, aligning evidence generation with program strategy and regulatory needs.
  • External Landscape Awareness: Maintain awareness of scientific, clinical, competitive, and regulatory developments that could impact the development plan and advise the team accordingly.
  • Publications: Support development of publications arising from internal studies and related initiatives, ensuring scientific rigor and clarity.
  • Business Development Support: Provide scientific support for due diligence and research collaborations to inform portfolio opportunities.

Essential Skills/Experience:
  • Advanced scientific degree (M.S., Ph.D., Pharm D., MPH or similar degree required)
  • 2+ years of experience in designing and executing clinical trials
  • Knowledge in the principles of literature search, clinical research methodology, statistics, data analysis and interpretation
  • Ability to communicate clearly to internal and external stakeholders
  • Experience in interacting with varying levels of internal/external management and/or academicians and/or clinicians and/or scientists

Desirable Skills/Experience:
  • Advanced knowledge of the therapeutic area (Rare Disease Cardiology & Amyloidosis)

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
Why AstraZeneca:
Here, mission meets momentum. You will work with clinicians, statisticians, data scientists, and operational experts who challenge each other in the same room to unlock new ideas that directly influence study decisions and, ultimately, patient outcomes. We combine the agility of innovative biotech teams with the resources and reach of a global biopharma, translating brave science into robust, ethical evidence at pace. We value kindness alongside ambition-your voice will be heard, your growth nurtured, and your impact felt in programs that matter to people and families living with devastating conditions.
Bring your scientific rigor and operational savvy to a team turning evidence into impact-share your resume today and help shape what comes next!
The annual base pay (or hourly rate of compensation) for this position ranges from $203,709.60 -$305,564.40 USD Annual. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
14-Aug-2026
Closing Date
13-Sep-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB

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