# Associate Director, Clinical Development Medical Director **Company**: Pfizer **Location**: Pennsylvania - Collegeville **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---Pennsylvania---Collegeville/Associate-Director--Clinical-Development-Medical-Director--MD-Required-_4967556?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply **Canonical**: https://yubhub.co/job/associate-director-clinical-development-medical-ff84d8ad-164/ ## Description The Associate Director, Clinical Development Medical Director is accountable for the medical and scientific integrity of a study and the wellbeing of patients enrolled in one or more clinical trials. The role involves ensuring the design of efficient and high-quality clinical trials, employing quantitative design principles and clinical best practices to deliver both clinical and operational excellence. Key responsibilities include: - Performing medical monitoring on one or more clinical trials - Providing study-related medical information and assistance - Contributing to final significant quality event medical assessments - Conducting and documenting periodic safety data reviews - Reviewing required safety text and endorsing significant medical changes in the Informed Consent Document - Leading or supporting development of the protocol from the approved Protocol Design Document (PDD) - Providing clinical/medical input to support development of the protocol design document (PDD) - Developing and implementing risk mitigations - Reviewing and approving country selection, developing site selection criteria - Serving as the primary contact with external investigators and internal study team for questions relating to clinical/medical aspects of protocol - Reviewing, reporting and managing protocol deviations - Tracking and reconciling serious adverse events (SAEs) across a study - Ensuring TMF compliance for clinical documents - Supporting disclosure of safety and efficacy data and trial conclusions - Contributing to primary publication of clinical trial results The ideal candidate has: - A primary medical degree (e.g., MD, DO, MBBS, MBChB) from a recognized medical school/university - Clinical Research experience in phase 3/pivotal space - Demonstrated scientific writing skills; scientific productivity via publications, posters, abstracts, and/or presentations - Been licensed by a licensing body/health authority to prescribe medicines independent of Supervision for at least 2 years post their intern/house officer/foundation period Preferred qualifications include: - Clinical Research experience in industry/CRO - Cardiometabolic disease experience - Extensive knowledge of clinical development, global and regional regulation, ICH/GCP, adverse event management - Demonstrated clinical/medical, administrative, and project management capabilities - Excellent verbal and written communication skills in English - Experience using common AI tools The annual base salary for this position ranges from $189,200.00 to $315,400.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 22.5% of the base salary and eligibility to participate in our share-based long-term incentive program. For more fresh new jobs, check out [yubhub.co](https://yubhub.co/). ## Skills ### Required - Clinical Research - Medical Writing - Protocol Development - Risk Management - Safety Reporting ### Nice to have - Cardiometabolic Disease Experience - AI Tools Experience - Clinical Development Knowledge - Project Management Capabilities --- Source: [Apply at pfizer.wd1.myworkdayjobs.com](https://pfizer.wd1.myworkdayjobs.com/en-US/PfizerCareers/job/United-States---Pennsylvania---Collegeville/Associate-Director--Clinical-Development-Medical-Director--MD-Required-_4967556?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)