Clinical Development Scientist, Director (Inflammation and Immunology)

Posted 20 Days Ago
Be an Early Applicant
Cambridge, MA, USA
Hybrid
177K-294K Annually
Senior level
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
The Clinical Development Scientist, Director will lead complex clinical trials in Inflammation and Immunology, ensuring scientific quality and patient safety. Responsibilities include protocol development, data interpretation, and implementing AI solutions in clinical workflows.
Summary Generated by Built In
POSITION SUMMARY
You will provide medical and scientific leadership for one or more complex clinical trials within our Inflammation and Immunology portfolio. You will be responsible for the clinical integrity, scientific quality, and patient safety of clinical studies, partnering closely with Clinical Operations and cross-functional stakeholders to deliver high-quality, efficient trials.
You will play a critical role in protocol development, study execution, data interpretation, and risk management, while serving as the primary clinical contact for investigators and internal study teams.
In addition, you will drive the integration of AI-enabled and advanced analytics solutions to transform clinical development workflows, improving speed, efficiency, and decision-making across the clinical trial lifecycle.
KEY RESPONSIBILITIES
Core Clinical Leadership
  • Lead the clinical execution of one or more medium- to high-complexity clinical studies
  • Provide clinical leadership in protocol design and development
  • Partner with Clinical Operations and cross-functional teams
  • Oversee clinical data review and safety surveillance
  • Serve as the primary clinical contact for stakeholders

AI-Enabled Clinical Development & Innovation
  • Lead identification and implementation of AI/ML and advanced analytics tools to optimize clinical trial design and execution]
  • Partner with Data Science, Digital, and Technology teams to translate AI use cases into scalable workflows
  • Champion adoption of innovative tools across study teams

Clinical Strategy and Deliverables
  • Contribute to clinical documents (protocols, CSRs, regulatory submissions)
  • Support risk management and safety review
  • Incorporate AI-derived insights and data-driven approaches into clinical strategy and regulatory deliverables where appropriate

MINIMUM QUALIFICATIONS
  • PhD/Pharm D in a relevant Science discipline and minimum of 5 years Clinical Research experience in the biopharmaceutical industry, OR
  • MS in a relevant Science discipline and minimum of 7 years of Clinical Research experience in the biopharmaceutical industry OR
  • BA/BS in a relevant Science discipline and minimum of 8 years Clinical Research experience in the biopharmaceutical industry
  • Deep knowledge of clinical development, ICH/GCP, global regulatory requirements, and safety management
  • Experience leading complex clinical studies and working effectively in cross‑functional, global teams
  • Strong written and verbal communication skills, with experience engaging internal and external stakeholders
  • Experience applying AI, machine learning, or advanced analytics in clinical development or research (e.g., protocol design and optimization, site selection and feasibility assessment, query management and workflow automation, data cleaning, anomaly detection, and signal identification, safety risk prediction and proactive mitigation)
  • Familiarity with AI-enabled use cases including protocol design, recruitment optimization, data review, and safety prediction
  • Experience partnering with data science or digital teams
  • Understanding of data governance and AI considerations in GxP environments

PREFERRED QUALIFICATONS
  • Advanced degree or professional certification in a scientific, medical, or healthcare related discipline
  • Experience in respiratory and/or dermatology therapeutic areas
  • Experience with real-world data, digital endpoints, or innovative clinical technologies

COMPETENCIES FOR SUCCESS
  • Promotes innovation and challenges the status quo
  • Embraces evolving technologies
  • Demonstrates intellectual curiosity and proactively explores emerging tools (including AI) to continuously improve and transform clinical development workflows
  • Demonstrates digital and data fluency, with ability to leverage AI tools responsibly and effectively
  • Balances innovation with patient safety, regulatory compliance, and scientific rigor
  • Demonstrates strong judgment and decision-making

Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.
PHYSICAL/MENTAL REQUIREMENTS
None
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Occasional travel may be required
Relocation support available
WORK LOCATION ASSIGNMENT: This is a hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week.
The annual base salary for this position ranges from $176,600.00 to $294,300.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.
Relocation assistance may be available based on business needs and/or eligibility.
Candidates must be authorized to be employed in the U.S. by any employer.
U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email [email protected] . This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Medical

Skills Required

  • PhD/Pharm D in relevant Science discipline and minimum of 5 years Clinical Research experience, OR MS in relevant Science and 7 years Clinical Research experience, OR BA/BS in relevant Science and 8 years Clinical Research experience
  • Deep knowledge of clinical development, ICH/GCP, global regulatory requirements, and safety management
  • Experience leading complex clinical studies
  • Strong written and verbal communication skills
  • Experience applying AI, machine learning, or advanced analytics in clinical development
  • Experience partnering with data science or digital teams

What the Team is Saying

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Pfizer

Pfizer Compensation & Benefits Highlights

  • Healthcare Strength Health coverage includes comprehensive medical with robust mental‑health networks, plus dental and vision options, and coverage for infertility/family‑building and transgender‑affirming care. Recent U.S. summaries name mental‑health partners and outline multiple plan choices.
  • Retirement Support The retirement program provides a 401(k) with company match plus an additional employer Retirement Savings Contribution, along with financial‑planning support and company‑paid life and disability insurance. These elements are highlighted as part of the core U.S. package.
  • Parental & Family Support Parental leave is described as up to 26 weeks in the U.S. when combining paid non‑medical parental leave with medical recovery where applicable, with exact pay and weeks dependent on circumstances and plan elections. Family‑building support includes egg preservation, adoption, and surrogacy coverage.

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The Company
HQ: New York, NY
121,990 Employees
Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.

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