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Clinical Science Manager Jobs (NOW HIRING)

Director, Clinical Science

Boston, MA · On-site

$86K - $118K/yr

... Management, Biostatistics, Clinical Pharmacology, Regulatory and Program Management, in the ... Attending scientific meetings pertinent to clinical science activities And will also include:

$86K - $118K/yr

Build organizational capability through talent planning, succession management, leadership ... Represent Clinical Science in governance forums, leadership discussions, and strategic planning ...

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Clinical Science Manager information

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$43.5K

$82.3K

$140K

How much do clinical science manager jobs pay per year?

As of Aug 11, 2026, the average yearly pay for clinical science manager in the United States is $82,350.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,000.00 and $89,500.00 per year, depending on experience, location, and employer.

How does a clinical science manager typically collaborate with cross-functional teams during clinical trial development?

Clinical Science Managers play a key role in bridging scientific objectives with operational execution by working closely with clinical operations, regulatory affairs, data management, and medical affairs teams. They often lead the development of clinical protocols and ensure scientific integrity throughout the study, facilitating regular meetings and communication to align project goals and timelines. Their collaborative efforts help anticipate and resolve challenges, streamline processes, and ensure that trials meet regulatory requirements and scientific standards.

What is a clinical science manager?

Clinical Science Managers are professionals who oversee and coordinate clinical research projects, often within the pharmaceutical, biotechnology, or medical device industries. They are responsible for managing clinical trials, ensuring regulatory compliance, and collaborating with cross-functional teams such as clinical operations, regulatory affairs, and medical affairs. Their role involves protocol development, data analysis, and ensuring the safety and efficacy of investigational products. Clinical Science Managers also play a critical part in interpreting study results and presenting findings to stakeholders. They typically have advanced degrees in life sciences and significant experience in clinical research.

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

AspectClinical Science ManagerClinical Research Associate
CredentialsTypically requires advanced degrees (e.g., Master’s or PhD) and industry experienceUsually holds a bachelor’s degree in life sciences or related field
Work EnvironmentLeads teams, manages projects, and oversees clinical studiesMonitors clinical trials at sites, ensures protocol compliance
Employer & Industry UsagePharmaceutical, biotech, and medical device companiesContract research organizations, pharmaceutical companies
Search & Comparison IntentUnderstanding managerial roles in clinical scienceFocus on trial monitoring and site management

The Clinical Science Manager typically oversees clinical projects and manages teams, requiring advanced credentials. In contrast, the Clinical Research Associate focuses on monitoring clinical trials at sites. Both roles are essential in the clinical research process but differ in responsibilities and experience levels.

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

To thrive as a Clinical Science Manager, you need a solid background in clinical research, life sciences, and project management, typically supported by an advanced degree (e.g., PharmD, PhD, or MD) and industry experience. Familiarity with clinical trial management systems, regulatory compliance tools, and data analysis platforms is crucial. Strong leadership, strategic thinking, and effective communication skills help you manage cross-functional teams and build relationships with stakeholders. These competencies ensure the successful design, execution, and oversight of clinical studies, ultimately advancing scientific and business goals.
More about Clinical Science Manager jobs
What cities are hiring for Clinical Science Manager jobs? Cities with the most Clinical Science Manager job openings:
What states have the most Clinical Science Manager jobs? States with the most job openings for Clinical Science Manager jobs include:
Infographic showing various Clinical Science Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 12% Part Time, and 1% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $82,350 per year, or $39.6 per hour.

Executive Director, Clinical Science, Immunology

MSD Malaysia

Rahway, NJ • On-site

$256 - $403/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 6 days ago


Job description

Job Description Brief Description of Position The Executive Director, Clinical Science is a senior leader within Non-Oncology Clinical Development responsible for providing strategic, scientific, operational, and people leadership across a portfolio of immunology programs spanning multiple stages of development. Reporting to the Head of Clinical Science Non-Oncology, this role serves as a member of the Clinical Science Leadership Team and plays a key role in shaping the strategic direction, operational effectiveness, and long-term growth of the Clinical Science organization. The Executive Director leads a large organization of Clinical Scientists supporting immunology development programs and is accountable for portfolio delivery, organizational performance, talent development, capability building, and continuous improvement. This leader ensures the highest standards of scientific rigor, patient focus, quality, and regulatory readiness while driving consistency and excellence across Clinical Science activities. The role champions innovation and modern ways of working by advancing the adoption of digital capabilities, advanced analytics, artificial intelligence, and data‑driven approaches that enhance decision‑making, improve efficiency, and strengthen study oversight across the portfolio. The Executive Director fosters a culture of learning, inclusion, accountability, and continuous improvement while developing future leaders and building organizational capability to meet evolving business needs. Success in this role requires strong enterprise leadership and effective collaboration across Clinical Operations, Regulatory Affairs, Biostatistics and Data Management, Drug Safety and Pharmacovigilance, Translational Medicine, Medical Affairs, and other key partner functions. The Executive Director influences across organizational boundaries to align priorities, integrate diverse perspectives, and enable successful execution of oncology development strategies.

Key Responsibilities
  • Portfolio Leadership Holds accountability for portfolio delivery from the Clinical Science perspective, including prioritization, resource alignment, and support for key development milestones across studies, programs, and assets. Provide strategic oversight for a portfolio of immunology assets across multiple stages of development. Partner withthe Immunology Therapeutic Area Head and leaders across Clinical Operations, Regulatory Affairs, Biostatistics and Data Management, Drug Safety and Pharmacovigilance, Translational Medicine, and Medical Affairs to drive development strategy execution and delivery of key portfolio milestones. Ensure Clinical Science contributions support development plans, regulatory submissions, health authority interactions, and lifecycle management activities. Apply Clinical Science expertise to inform therapeutic area and portfolio strategy across evolving science, treatment trends, competitive landscape, and regulatory considerations. Optimize allocation of Clinical Science resources and associated budgets across a complex and evolving portfolio to align with business priorities and organizational objectives. Serve as a senior escalation point for scientific, and resource‑related issues, enabling effective and timely resolution.
  • Clinical Science Excellence Establish and sustain high standards for scientific rigor, clinical science quality, medical data review, study oversight, and regulatory readiness across the portfolio. Drive consistency in clinical science practices, study execution, and data interpretation across therapeutic areas and development programs. Foster a culture of proactive risk identification, mitigation, inspection readiness, and continuous quality improvement. Advance innovative approaches to medical data review, signal detection, study oversight, and evidence‑based decision‑making that enhance development outcomes.
  • Innovation, AI, and Digital Transformation Champion adoption of AI‑enabled, digital, and technology‑driven capabilities that enhance Clinical Science productivity, quality, efficiency, and effectiveness. Contribute to identifying opportunities to leverage advanced analytics, artificial intelligence, automation, and digital solutions to improve decision‑making, strengthen study oversight, and streamline workflows. Drive modernization of clinical data review through innovative approaches that enhance insight generation and support timely, informed decisions. Foster a culture of innovation, experimentation, continuous learning, and responsible implementation of emerging technologies. Partner with cross‑functional stakeholders to define, develop, and implement scalable capabilities that support future organizational needs and long‑term business success.
  • People Leadership and Talent Development Lead, coach, and develop a high‑performing Clinical Science organization. Build organizational capability through talent planning, succession management, leadership development, and career growth strategies. Create an inclusive environment that promotes engagement, psychological safety, accountability, collaboration, and continuous development. Develop future leaders by mentoring Clinical Scientists, strengthening scientific, strategic, and leadership capabilities across the organization. Ensure leaders are equipped to provide effective coaching, feedback, performance development, and career support for their teams.
  • Organizational Leadership Contribute to the development and execution of Clinical Science strategy, priorities, and long‑term organizational objectives. Lead initiatives related to organizational design, workforce planning, and resource optimization to support evolving portfolio and business needs. Develop and implement scalable operating models that balance portfolio execution, organizational effectiveness, employee development, and talent retention. Lead cross‑functional initiatives that improve efficiency, effectiveness, innovation, and organizational health. Represent Clinical Science in governance forums, leadership discussions, and strategic planning activities. Shape functional and enterprise priorities through leadership engagement, cross‑functional partnerships, and influence across organizational boundaries.
Qualifications, Skills & ExperienceEssential Leadership Skills
  • Generate and consider options for action to achieve a long‑range goal; develop decision criteria considering factors, such as cost, benefits, risks, timing and buy‑in; select the strategy most likely to succeed.
  • Identify the key tasks and resources needed to achieve strategic objectives.
  • Offer a broad organizational perspective that goes beyond the goals of one’s immediate business unit or work role; question assumptions about existing relationships; demonstrate flexibility when forming and adjusting partnerships to achieve broader goals; show willingness to work across current boundaries.
  • Ensure that those responsible for implementing a strategic initiative have role clarity and accountability for required actions and outputs, as well as the direction and authority to act in a way consistent with organizational values.
  • Leverage environmental supports and remove development barriers; advocate for individual to higher levels of management to create development opportunities; provide guidance and positive models; seek suggestions for improving performance; collaboratively create development plans that include activities targeted to specific goals.
  • Create momentum by taking immediate action and encouraging others to take action to improve organizational culture, processes or products/services; offer resources and direction to support implementation; break down cultural and operational barriers to change; recognize and reward those who contribute to change efforts.
Education

Advanced scientific or healthcare degree (e.g., PhD, PharmD) with at least 10 years of drug development experience; OR Master’s degree, preferably in a life sciences‑related field, with at least 15 years of drug development experience.

Experience

Significant experience in drug development with demonstrated success across multiple phases of clinical development. Deep expertise in Clinical Science, Clinical Development, and execution of global clinical programs. Experience supporting regulatory submissions, health authority interactions, and late‑stage development activities. Proven leadership experience managing in large, matrixed organizations through multiple levels of management. Demonstrated success developing talent, building leadership capability, and creating high‑performing teams. Familiarity with, or interest in emerging AI, advanced analytics, and digital capabilities applicable to clinical development. Experience in immunology development strongly preferred.

Required Skills
  • Advanced Analytics
  • Artificial Intelligence (AI)
  • Clinical Development
  • Clinical Sciences
  • Cross‑Functional Leadership
  • Drug Development
  • Executive Leadership
  • Global Clinical Studies
  • Immunology
  • Innovation
  • Matrix Leadership
  • Regulatory Submissions
  • Strategic Leadership
  • Talent Development
Preferred Skills

[No preferred skills listed]

US and Puerto Rico Residents Only

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities.

Equal Employment Opportunity Statement

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement. We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts.

Compensation and Benefits

The salary range for this role is $255,800.00 - $402,700.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long‑term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

Location

UG/RY/Boston/South San Francisco

Travel

0-25%

Employment Information
  • Employee Status: Regular
  • Relocation: Domestic
  • VISA Sponsorship: No
  • Travel Requirements: 25%
  • Flexible Work Arrangements: Hybrid
  • Shift: Not Indicated
  • Valid Driving License: No
  • Hazardous Material(s): n/a
Closing Date

Job Posting End Date: 08/24/2026

Company Overview

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

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