Clinical Director Jobs in Waltham, MA
Clinical Director jobs in Waltham are in strong demand, concentrated in the Waltham Watch Factory district, Bear Hill, and the Route 128 corridor, across behavioral health, life sciences, and hospital systems. Employers hiring right now include AbbVie, Alkermes, and CSL. See the openings below and apply to the ones that match your experience.
Find Clinical Director JobsOverview
Showing 5 of 169+ Clinical Director jobs
Entity: CSL Behring
Job Category: Physicians
Job Family: Research & Medical Affairs
Job Type: Full Time
Location: Waltham, Massachusetts, United States
Employer Reference: R-293920
Job Description
Position Overview:
The Senior Medical Director, Global Clinical Program Leader (GCPL) is a critical role within Clinical Development. The Senior GCPL is
accountable for the design and execution of the clinical strategy to support the development of a medicine, aligned with the Project Strategy Document (PSD) and the Target Product Profile (TPP). The GCPL is accountable for the strategic leadership of the Clinical Development Team (CDT) in a matrixed environment. Reports to the Global Clinical Lead (GCL).
Work Environment:
*** This is a hybrid position based onsite at any of the posted locations with a minimum of 3 days onsite weekly. Relocation assistance and visa sponsorship are not provided.
Key Resonsibilities:
Clinical Development Team (CDT) Leadership:
- Provides leadership and guidance to all members of the cross-functional CDT acting as the lead scientific expert for the clinical program, while ensuring appropriate functional representation in team discussions
- accountable for the timely development and maintenance of the Clinical Development Plan (CDP) in alignment with the Program Strategy Team (PST) and Therapeutic Area Leadership Team (TALT)
- Leads the integration of internal and external expert contributions to strategy and design of the assigned clinical program(s)
- Maintaining alignment across critical stakeholders prior to key decision making forums (e.g. Strategic Development Committee (SDC) or Scientific and Technical Review Committee (STRC) for study outline approval)
- Ensures that the program is conducted in alignment with CSL Behring processes and abiding by GCP and ICH regulations
- Responsible for driving and documenting decision making within the CDT, facilitating issue resolution and escalation, as well as contingency planning
Clinical & Scientific Oversight:
- Accountable for the clinical content for all CDT deliverables to ensure safe, efficient, timely and quality execution of assigned clinical programs
- Ensures high quality clinical and scientific standards are met throughout all aspects of the program
- Serves as the clinical development representative on the required cross-functional teams, including but not limited to the Study Execution Team (SET), Safety Management Team (SMT), the Benefit-Risk Assessment Team (BRAT), the Biomarker Expert Team (BET), and the Evidence and Access Strategy Team (EAST) for assigned programs
- Develops and executes the Medical Monitoring Plan (MMP) strategy
- Typically serves as the medical monitor for clinical trials during study conduct or provides oversight to assigned medical monitors
- Presents results to Safety Monitoring Committee and other internal and external meetings
- May participate or lead Due Diligence projects in support of CSL’s external innovation efforts
Document Authorship:
- Reviews the data generated during the planning and execution of a study to gather a clinical understanding of the safety and efficacy results and the impact of the data on ongoing R&D strategies and provides support in defining the development strategy
- “Lead Author” or “Contributing” Author for key study documents, including but not limited to: the TPP, PSD, CDP, Study Concept Scenarios, Study Outlines, the Investigator Brochure (IB), Clinical Study Protocols (CSP), Master Informed Consent Forms (ICF), Medical Monitoring Plans (MMP), Safety Review Committee (SRC)/Independent Data Monitoring Committee (IDMC) Charters, and Clinical Study Reports (CSR)
- Leads preparations of clinical sections of relevant regulatory interaction packages including but not limited to briefing books, INDs, NDAs. BLAs, ODDs, RFIs, and routine reporting
- Contributing author the publication strategy. Author or contributing author for abstracts, presentations, and manuscripts as appropriate
Minimum Qualifications:
- MD, PhD or PharmD in life science/healthcare discipline expected. MD - Board Certified (or non-USA equivalent) in relevant field is preferred.
- 5+ years of relevant clinical development experience in the pharmaceutical industry is expected including experience with study data review/evaluation
- Clinical development industry experience with a working knowledge of pharmaceutical and regulatory development processes is essential
Demonstrated program leadership capabilities in a matrixed environment - Demonstrated stakeholder management skills including risk mitigation
- Proficient in project management terminology and processes to drive clinical development program risk mitigation strategies
- Excellent analytical thinking and scientific/medical writing skills
- Proficient in clinical data analysis and interpretation
- Proven effective problem-solving skills and the ability to think critically and make informed decisions
- Demonstrated effective communication and presentation skills Proven ablility to build bridges and proactively improve cross-functional collaboration
-
The minimum and maximum base salary range that CSL expects to pay for this position at the Waltham, MA USA work location at the time of this posting is $317,000 - $409,000/yr. Individual base salary for a successful candidate is determined by qualifications, skill level, experience, competencies and other relevant factors. In addition to base salary, total compensation for this role may also include incentive compensation and equity.
#LI-HYBRID
About CSL Behring
CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients' needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.
CSL Behring operates one of the world's largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.
To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.
Our Benefits
For more information on CSL benefits visit How CSL Supports Your Well-being | CSL.
You Belong at CSL
At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.
To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging
Equal Opportunity Employer
CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.
Entity: CSL Behring
Job Category: Physicians
Job Family: Research & Medical Affairs
Job Type: Full Time
Location: Waltham, Massachusetts, United States
Employer Reference: R-293920
Job Description
Position Overview:
The Senior Medical Director, Global Clinical Program Leader (GCPL) is a critical role within Clinical Development. The Senior GCPL is
accountable for the design and execution of the clinical strategy to support the development of a medicine, aligned with the Project Strategy Document (PSD) and the Target Product Profile (TPP). The GCPL is accountable for the strategic leadership of the Clinical Development Team (CDT) in a matrixed environment. Reports to the Global Clinical Lead (GCL).
Work Environment:
*** This is a hybrid position based onsite at any of the posted locations with a minimum of 3 days onsite weekly. Relocation assistance and visa sponsorship are not provided.
Key Resonsibilities:
Clinical Development Team (CDT) Leadership:
- Provides leadership and guidance to all members of the cross-functional CDT acting as the lead scientific expert for the clinical program, while ensuring appropriate functional representation in team discussions
- accountable for the timely development and maintenance of the Clinical Development Plan (CDP) in alignment with the Program Strategy Team (PST) and Therapeutic Area Leadership Team (TALT)
- Leads the integration of internal and external expert contributions to strategy and design of the assigned clinical program(s)
- Maintaining alignment across critical stakeholders prior to key decision making forums (e.g. Strategic Development Committee (SDC) or Scientific and Technical Review Committee (STRC) for study outline approval)
- Ensures that the program is conducted in alignment with CSL Behring processes and abiding by GCP and ICH regulations
- Responsible for driving and documenting decision making within the CDT, facilitating issue resolution and escalation, as well as contingency planning
Clinical & Scientific Oversight:
- Accountable for the clinical content for all CDT deliverables to ensure safe, efficient, timely and quality execution of assigned clinical programs
- Ensures high quality clinical and scientific standards are met throughout all aspects of the program
- Serves as the clinical development representative on the required cross-functional teams, including but not limited to the Study Execution Team (SET), Safety Management Team (SMT), the Benefit-Risk Assessment Team (BRAT), the Biomarker Expert Team (BET), and the Evidence and Access Strategy Team (EAST) for assigned programs
- Develops and executes the Medical Monitoring Plan (MMP) strategy
- Typically serves as the medical monitor for clinical trials during study conduct or provides oversight to assigned medical monitors
- Presents results to Safety Monitoring Committee and other internal and external meetings
- May participate or lead Due Diligence projects in support of CSL’s external innovation efforts
Document Authorship:
- Reviews the data generated during the planning and execution of a study to gather a clinical understanding of the safety and efficacy results and the impact of the data on ongoing R&D strategies and provides support in defining the development strategy
- “Lead Author” or “Contributing” Author for key study documents, including but not limited to: the TPP, PSD, CDP, Study Concept Scenarios, Study Outlines, the Investigator Brochure (IB), Clinical Study Protocols (CSP), Master Informed Consent Forms (ICF), Medical Monitoring Plans (MMP), Safety Review Committee (SRC)/Independent Data Monitoring Committee (IDMC) Charters, and Clinical Study Reports (CSR)
- Leads preparations of clinical sections of relevant regulatory interaction packages including but not limited to briefing books, INDs, NDAs. BLAs, ODDs, RFIs, and routine reporting
- Contributing author the publication strategy. Author or contributing author for abstracts, presentations, and manuscripts as appropriate
Minimum Qualifications:
- MD, PhD or PharmD in life science/healthcare discipline expected. MD - Board Certified (or non-USA equivalent) in relevant field is preferred.
- 5+ years of relevant clinical development experience in the pharmaceutical industry is expected including experience with study data review/evaluation
- Clinical development industry experience with a working knowledge of pharmaceutical and regulatory development processes is essential
Demonstrated program leadership capabilities in a matrixed environment - Demonstrated stakeholder management skills including risk mitigation
- Proficient in project management terminology and processes to drive clinical development program risk mitigation strategies
- Excellent analytical thinking and scientific/medical writing skills
- Proficient in clinical data analysis and interpretation
- Proven effective problem-solving skills and the ability to think critically and make informed decisions
- Demonstrated effective communication and presentation skills Proven ablility to build bridges and proactively improve cross-functional collaboration
-
The minimum and maximum base salary range that CSL expects to pay for this position at the Waltham, MA USA work location at the time of this posting is $317,000 - $409,000/yr. Individual base salary for a successful candidate is determined by qualifications, skill level, experience, competencies and other relevant factors. In addition to base salary, total compensation for this role may also include incentive compensation and equity.
#LI-HYBRID
About CSL Behring
CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients' needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.
CSL Behring operates one of the world's largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.
To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.
Our Benefits
For more information on CSL benefits visit How CSL Supports Your Well-being | CSL.
You Belong at CSL
At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.
To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging
Equal Opportunity Employer
CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.
See All 169+ Clinical Director Jobs in Waltham
Find roles in Waltham that match your experience and apply in just a few clicks.
Find Clinical Director JobsClinical Director Job Market in Waltham
Who's Hiring
- AbbVie70
- Alkermes35
- CSL21
- Nova Biomedical14
- Deciphera Pharmaceuticals14
Top Industries Hiring
- Biotechnology & Pharmaceuticals
Clinical Director Jobs in Waltham: Frequently Asked Questions
How do I get a clinical director job in Waltham?
The strongest path into a clinical director role in Waltham runs through the city's behavioral health providers, specialty care clinics, and life sciences companies along the Route 128 corridor. Candidates with hands-on experience managing multidisciplinary teams and a history of regulatory compliance tend to stand out. Familiarity with value-based care models and population health platforms gives applicants a concrete edge with Waltham's integrated health networks.
Which companies hire clinical directors in Waltham?
Employers hiring clinical directors in Waltham right now include AbbVie, Alkermes, and CSL, based on current listings on Migrate Mate as of October 2026. Waltham's mix of hospital-affiliated outpatient centers, digital health companies, and specialty behavioral health organizations means clinical director openings appear across a broader range of employer types than in many comparable cities.
Are there remote clinical director jobs in Waltham?
Yes, though with limits: clinical director roles that involve direct patient oversight or on-site staff management are mostly in-person by nature, while quality improvement, compliance, and telehealth-focused director positions are more remote-compatible. About 90% of clinical director openings tied to Waltham are remote or hybrid as of October 2026. The most remote-eligible positions in Waltham tend to sit within digital health and managed care organizations in the Route 128 corridor.
How can I get a clinical director job in Waltham with little or no experience?
The most realistic entry path in Waltham is moving into a clinical supervisor or program manager role first, particularly with one of the city's outpatient behavioral health agencies or specialty care clinics, which tend to promote from within. Gaining experience with outcomes reporting and quality metrics matters to Waltham's life sciences-adjacent health employers. Volunteering for accreditation or compliance projects internally can accelerate the transition into a director-level title.
Which industries hire the most clinical directors in Waltham?
Waltham clinical director roles concentrate in Biotechnology & Pharmaceuticals, based on current listings on Migrate Mate as of October 2026. Waltham's dense cluster of biotech and digital health firms along Route 128, combined with its established behavioral health and outpatient care infrastructure, makes it one of Greater Boston's more active markets for senior clinical leadership outside of the main hospital campuses.
Related Jobs in Massachusetts
See All 169+ Clinical Director Jobs in Waltham
Find roles in Waltham that match your experience and apply in just a few clicks.
Find Clinical Director Jobs