Clinical Development Scientist, Senior Manager

Pfizer Inc; United States; On-site; USD 150,000 - 210,000; Full time

Benefits offered by this job

Relocation support available

Job summary

Pfizer Inc. is seeking a Senior Manager, Clinical Development Scientist in Internal Medicine to provide scientific oversight, ensure data integrity, and drive quality across one or more studies.

You will mentor team members and contribute to protocol development, safety planning, and regulatory submissions. Responsibilities include leading clinical deliverables, collaborating with investigators and health authorities, and supporting data review, TMF compliance, and study reporting.

Qualifications

• Science degree (PhD, PharmD, or equivalent) with at least 1 year, or MA/MS with at least 5 years, or BA/BS with at least 6 years of Clinical Research experience in a similar role in the biopharmaceutical industry.
• 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.

Responsibilities

• Provides clinical support for one or more studies; may be accountable for program level clinical deliverables
• May provide input to the protocol design document; contributes to development of the protocol, including protocol amendments, Protocol Administrative Change Letters, and Dear Investigator Letters
• Supports the study team in internal protocol review governance submissions and interactions; supports the Global Development Lead in study and disease area strategy; may participate in protocol-related KOL and Health Authority interactions
• May develop Study Informed Consent Documents and responses to external stakeholder requests (e.g., Health Authority and Independent Ethics Committee)
• Provides clinical input to the development of the Statistical Analysis Plan and Tables, Listings, and Figures
• Provides clinical input to the development of the clinical data collection strategy, instruments, and data review plan, ensuring alignment with the protocol and SAP, optimized data collection principles, and clinical data review best practice
• Performs clinical data review; may present data to internal and external stakeholders; partners with site-facing colleagues in support of data issue resolution; ensures all clinical queries are addressed in support of database lock
• Provides clinical input to the development of the Safety Review Plan and Safety Narrative Plan; reviews safety data and may update clinical documents in response to emerging safety profile; tracks and reconciles Serious Adverse Events; participates in safety data discussions during Safety Review Team meetings
• Provides clinical input to the development of the Risk Management Plan; conducts clinical activities consistent with the approved Plan and partners with key stakeholders to develop and implement risk mitigations
• Supports establishment and management of External Data Monitoring Committees and Adjudication Committees; including chartering, contracting, provision and presentation of data, and documentation and dissemination of Committee recommendations
• Contributes to site selection criteria, provides clinical input to selection of sites, and may deliver protocol training to site-facing colleagues
• Participates in investigator meeting planning and may develop and deliver protocol training; may develop and deliver ongoing protocol training in response to amendments, data issues, and quality events
• May serve as a clinical point of contact with investigators and study team for questions relating to clinical aspects of the protocol; contributes to clinical response development and curation
• May author protocol deviation sub-categories; ensures protocol deviations identified during clinical data review are reported; ensures all reported deviations are managed and reconciled
• Ensures TMF compliance for clinical documents
• Provides clinical input and review of the Clinical Study Report
• Provides clinical support to disclosure of safety and efficacy data and trial conclusions; may contribute to publications
• Provides clinical support to audits and inspections, including responding to audit and inspection findings
• May contribute to clinical sections of regulatory filings (e.g., Briefing Documents, Pediatric Investigational Plan, Investigator Brochure, IND/NDA Annual Reports, PSURs)
• Contributes to continuous improvement / process enhancement activities and innovative approaches to maximize effectiveness of clinical trial execution
• May supervise, mentor, or develop others

Education

Science degree (PhD, PharmD, or equivalent)

MA/MS with at least 5 years of Clinical Research experience

BA/BS with at least 6 years of Clinical Research experience

Job description

The Clinical Development Scientist (Senior Manager) is responsible for scientific oversight, data integrity, and quality of clinical trials in Internal Medicine, with direct responsibility for clinical deliverables for one or more studies. They may also supervise and mentor others.

JOB RESPONSIBILITIES

• Provides clinical support for one or more studies; may be accountable for program level clinical deliverables
• May provide input to the protocol design document; contributes to development of the protocol, including protocol amendments, Protocol Administrative Change Letters, and Dear Investigator Letters
• Supports the study team in internal protocol review governance submissions and interactions; supports the Global Development Lead in study and disease area strategy; may participate in protocol-related KOL and Health Authority interactions
• May develop Study Informed Consent Documents and responses to external stakeholder (e.g., Health Authority and Independent Ethics Committee) requests
• Provides clinical input to the development of the Statistical Analysis Plan and Tables, Listings, and Figures
• Provides clinical input to the development of the clinical data collection strategy, instruments, and data review plan, ensuring alignment with the protocol and SAP, optimized data collection principles, and clinical data review best practice; performs clinical data review; may present data to internal and external stakeholders; partners with site-facing colleagues in support of data issue resolution; ensures all clinical queries are appropriately addressed in support of database lock
• Provides clinical input to the development of the Safety Review Plan and Safety Narrative Plan; reviews safety data and may update clinical documents in response to emerging safety profile; tracks and reconciles Serious Adverse Events; participates in clinical safety data discussion during Safety Review Team meetings in collaboration with Medically Qualified Individual(s); reviews safety narratives
• Provides clinical input to the development of the Risk Management Plan; conducts clinical activities consistent with the approved Plan and partners with key stakeholders to develop and implement risk mitigations
• Supports establishment and management of External Data Monitoring Committees and Adjudication Committees, including chartering, contracting, provision and presentation of data, and documentation and dissemination of Committee recommendations
• Contributes to site selection criteria, provides clinical input to selection of sites, and may deliver protocol training to site-facing colleagues
• Participates in investigator meeting planning and may develop and deliver protocol training; may develop and deliver ongoing protocol training in response to e.g., protocol amendments, emerging data issues, and quality events
• May serve as a clinical point of contact with investigators and study team for questions relating to clinical aspects of the protocol; contributes to clinical response development, delivery, documentation, and curation (e.g., in FAQ)
• May author protocol deviation sub-categories; ensures protocol deviations identified during clinical data review are reported; ensures all reported protocol deviations are appropriately managed and reconciled; may lead protocol deviation trends review
• Ensures TMF compliance for clinical documents
• Provides clinical input and review of the Clinical Study Report
• Provides clinical support to disclosure of safety and efficacy data and trial conclusions; may contribute to publications
• Provides clinical support to audits and inspections, including responding to and addressing audit and inspection findings
• May contribute to clinical sections of regulatory filings (e.g., Briefing Documents, Pediatric Investigational Plan, Investigator Brochure, IND/NDA Annual Reports, Periodic Safety Update Reports, responses to Health Authority requests)
• Contributes to continuous improvement / process enhancement activities and innovative approaches to maximize effectiveness of clinical trial execution
• May supervise, mentor, or develop others

BASIC QUALIFICATIONS

• Science degree (PhD, PharmD, or equivalent) with at least 1 year, or MA/MS with at least 5 years, or BA/BS with at least 6 years of Clinical Research experience in a similar role in the biopharmaceutical industry
• 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.
• Relocation support available

PREFERRED QUALIFICATIONS

• Cardiometabolic disease experience, e.g., obesity, diabetes, endocrinology, etc.
• Clinical research experience in the biopharmaceutical industry in study design, start-up, conduct,and close-out, including regulatory submissions and inspections
• Scientific productivity via publications, posters, abstracts and/or presentations
• Knowle