1+ months

Associate Director, Medical Monitor VRD

Collegeville, PA 19426
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The Clinician Medical Monitor (CMM) is accountable for providing medical and scientific expertise and oversight for Global Clinical Trials and serves as a single point of accountability for design, execution, monitoring, delivery and reporting of one or more clinical studies to ensure patient safety. Additional study level activities include presentation of study results to internal and external committees or advisory boards, presentation of data at international scientific meetings and publication of study results in peer reviewed journals.

The CMM will also act as a medical monitor for select clinical trials, including phase 2B and phase 3 registration studies, The CMM is accountable for patient safety for subjects participating in Pfizer clinical trials and provides medical guidance during the design, execution, and reporting for clinical studies.

In addition to study level activities, the CMM will participate in program level activities including authoring/reviewing safety and efficacy summaries, clinical overviews, investigator brochures, risk management plans, periodic safety update and clinical sections of product labels.

In addition to work on specific assets the CMM will participate in standing committees, review compounds for potential in-licensing, including performance of due diligence reviews, and provide assistance to new business development on market opportunities and the target product profile.



In collaboration with GCPL, and Pfizer Vaccine Clinical Research and Development Operations colleagues and Alliance Partners, conduct the design of clinical studies to meet the stated objectives. Directs Clinical Scientists (CSs) in writing the synopsis and protocol

Approve and be accountable for protocols and amendments

Approve informed consents

Provide medical input into investigational site feasibility

Coordinate with the CS to review and approve processes for data capture and review

In conjunction with GCPL and Pfizer colleagues, organizing expert panels or consultant or advisory board meetings to provide input into clinical development plans, protocols and data analyses


Protocol training for investigators

Issue resolution

Audit responses

Study closeout

Inspection Readiness

Review Informed Consent Forms (ICFs)


Ensures development of and adherence to Safety Review Plan (SRP). Consistent with SRP, performs and documents regular review of individual subject safety data, and performs review of cumulative safety data with the safety risk lead.

As appropriate, the Clinician (MD) may delegate these responsibilities to the study clinical scientist identified in the SRP.

The specific components of safety data review are detailed in the Safety Data Review Guide - for Clinicians and in SAF09 SOP.

Review individual subject data (including AEs and other safety data), SAEs, and potentially clinically important findings as well as determining if follow up is needed

Participate in Safety Review Team (SRT), interact with Data Monitoring Committee (DMC)

Provide responses to questions on safety: reviews literature as needed to respond to safety questions or those posed by the SRT, DMC or other individuals or bodies involved with the study


Perform review of data generated by statistical analyses

Request additional tables or analyses as indicated

Perform reviews and procedures required for database finalization

Authors Clinical Study Reports

Authors clinical sections of regulatory documents (e.g., Investigator Brochure (IB), IND Annual Reports)


General protocol questions, questions on inclusion/exclusion, etc.

Ensures answers are consistent across study regions

Interact with regulatory authorities and internal regulatory and auditing groups on a study level

Data Monitoring Committee

Support RA interaction, accountable for providing responses to RA inspection observations and internal audits

Support RA updates and registration submissions


Steering Committee

Clinical trial efficacy endpoint Adjudication Committee


Under the direction of GCPL and/or CTL, prepare and deliver reports of clinical trial results to Pfizer committees as well as to regulatory authorities and external medical and scientific committees or conferences.


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.

MD degree

Licensed by a health authority to prescribe medicines (independent of supervision) for at least one year (post "intern/houseman" year), and has utilized the license to prescribe medicines in a patient care setting for an aggregate duration of at least one year.

M.D. required, internal medicine or surgical certification is highly desirable. Training and experience in infectious diseases or infection control experience in the hospital setting is preferred

Knowledge of Good Clinical Practice

Experience in small molecule or vaccine clinical development and conduct of clinical trials for treatment or prevention of diseases in hospitalized patients is preferred

Experience in assessment of adverse events and safety among hospitalized patients participating in therapeutic clinical trials is preferred

Skilled in protocol design, interpretation, and medical monitoring

General therapeutic area knowledge

Excellent written and oral communication

Capacity to adapt to a fast-pace and changing environment


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.

Some travel may be required for this position.

**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.


Posted: 2021-04-23 Expires: 2021-06-28
Sponsored by:
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Associate Director, Medical Monitor VRD

Collegeville, PA 19426

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