# Clinician

**Company**: Pfizer
**Work arrangement**: hybrid
**Experience**: senior
**Job type**: full-time
**Salary**: $189,200.00 to $315,400.00
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://pfizer.wd1.myworkdayjobs.com/en-US/PfizerCareers/job/United-States---New-York---Pearl-River/Clinical-Development-Medical--Associate-Director_4965916-2?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_74252d0f-278

## Description

The primary purpose of this role is to serve as a Clinician within a Pfizer vaccine development program.

You will work closely with the global clinical program lead and serve as a clinical lead for one or more studies within a clinical program.

Your responsibilities will include:

**Accountable for safety across the study**

- Providing medical advice for all medical issues during risk assessment and mitigation planning

- Ensuring development of and adherence to the Safety Surveillance Review Plan (SSRP)

- Monitoring study safety issues and providing input to serious adverse events (SAEs) reports

- Participating in the Safety Review Team to evaluate medical benefits/risks

- Reviewing literature as needed to respond to safety questions

- Communicating safety information to sites across the study

**Protocol design and strategy**

- Contributing towards medical input during protocol development and updates to the clinical development plan

- Working closely with other medical monitors to ensure documents meet regulatory requirements and company policy

- Providing medical input into country feasibility

**Support study team**

- Providing clinical input to protocol/study team for monitoring guidelines, statistics analysis plans, and data quality planning

- Contributing to contract research organization/vendor selection

- Working with study team to ensure high-quality data

- Contributing to medical review and interpretation of efficacy and safety data

- Providing protocol-specific training to study team, investigators, and clinical research associates

- Interacting with healthcare professionals at sites during the conduct of the study

**Supports the program team**

- Authoring clinical sections of regulatory documents

- Co-authoring abstracts, posters, presentations, and publications

- Contributing to budget execution of protocols

**Interact with regulatory authorities, key opinion leaders, and principal investigators**

- Supporting Clinical Regulatory Authority interactions

- Liaising with Key Opinion Leaders and Principal Investigators in countries

**Basic qualifications:**

- Medical degree (M.D./D.O. or equivalent)

- Licensed by a health authority to prescribe medicines (independent of supervision) for at least one year

- 0-4 years' work experience

- Ability to critically evaluate medical/scientific information

- Excellent written and oral communication

- Understanding of the design, development, and execution of clinical programs and studies

- Capacity to adapt to a fast-paced and changing environment

- Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot

- Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices

**Preferred qualifications:**

- Documented work experience/knowledge of statistics

- Training and experience in infectious diseases and/or infection control in the hospital setting

- Experience with investigational clinical trials

**Additional details:**

- Hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week

- Annual base salary ranging from $189,200.00 to $315,400.00

- Eligible for participation in Pfizer's Global Performance Plan and share-based long-term incentive program

- Comprehensive benefits package, including 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

## Skills

### Required
- Medical degree
- Clinical trials
- Medical monitoring
- Regulatory compliance
- AI tools

### Nice to have
- Statistics
- Infectious diseases
- Infection control
- Investigational clinical trials

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Source: [Apply at pfizer.wd1.myworkdayjobs.com](https://pfizer.wd1.myworkdayjobs.com/en-US/PfizerCareers/job/United-States---New-York---Pearl-River/Clinical-Development-Medical--Associate-Director_4965916-2?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)