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高级/执行医学主任 - MD 美国远程办公

Sr / Executive Medical Director - MD US Remote Based

其他限定地区(需当地身份)
公司Lifelancer
薪资$173,000 - $320,000/年
工作地点United States
地域资格限定地区(需当地身份)
时区要求日间重叠约 9 小时,基本正常作息
用工类型Full Time
发布时间14 天前
数据来源Himalayas
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注意地域限制:该职位明确限定在 United States 招聘。如果你是位于中国大陆的求职者,通常需要当地工作身份才能投递,或需与雇主确认是否接受独立合同(Contractor)形式合作。

职位名称:高级医学总监 / 执行医学总监 - 美国远程办公
工作地点:达勒姆
工作地点类型:远程
工作合同类型:全职
职位级别:高级医学总监 / 执行医学总监
美国远程办公

Fortrea 正在寻找一位高级医学总监或执行医学总监,为客户提供医学领导力和战略支持,同时与客户和跨职能团队合作,加强关系并推动成功的临床开发项目。该职位将对团队成员提供监督、指导和建议,并参与全球临床运营的关键项目。理想的候选人是一位具有深厚临床研究经验、强大临床判断力,并致力于提升患者护理和创新疗法的协作型领导者。

此职位发布是为了未来可能在 Fortrea 出现的机会。

主要职责

  • 参与公司涉及医学、安全性和治疗领域的政策制定。
  • 参与公司范围内的流程改进活动。
  • 为治疗领域内的员工提供领导力。
  • 领导影响并涉及治疗领域内和跨治疗领域的医生的项目。
  • 可能参与治疗领域的愿景和战略方向的制定。
  • 开发培训模块和材料,并在公司范围内提供疾病状态和方案特定要求的培训。
  • 参与培训机会,以提升药物开发和良好临床实践(GCP)指南的知识。
  • 作为关键成员,为客户的医学策略和执行提供专业领域和药物开发专业知识。
  • 制定、审查和修订方案、病例报告表、培训材料、项目专用工具、分析计划设计、临床试验报告和新药申请。
  • 为项目团队提供医学和科学专业知识。
  • 作为医学监查员/研究支持人员,根据方案或项目进行早期临床试验的医学和安全监测,并负责所分配项目的医学和安全监测。
  • 与内部部门团队和外部顾问进行适当互动。
  • 参与特定项目提案的可行性讨论。
  • 参与项目风险评估活动。
  • 在需要时协助数据安全监控委员会的工作。
  • 提供临床和医学专家意见
查看英文原文

Job Title: Sr / Executive Medical Director - MD US Remote Based
Job Location: Durham
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:
Senior Medical Director / Executive Medical Director
US Remote Based

Fortrea is seeking a Senior Medical Director or Executive Medical Director to provide medical leadership and strategic support while partnering with clients and cross-functional teams to strengthen relationships and drive successful clinical development programs. This role will provide oversight, mentorship, and guidance to team members while contributing to key initiatives across Global Clinical Operations. The ideal candidate is a collaborative and influential leader with deep clinical research expertise, strong clinical judgment, and a passion for advancing patient care and innovative therapies.

This posting is intended for future opportunities that may arise at Fortrea.

Key / Core Responsibilities

  • Contributes to the development of Company policies involving medical, safety, and therapeutics.
  • Participates in process improvement activities across the Company.
  • Provides leadership to staff within the therapeutic area.
  • Leads initiatives that impact and involve physicians within and across the therapeutic area.
  • May contribute to the vision and strategic direction of the therapeutic area.
  • Develops training modules and materials and provides training in disease states and protocol-specific requirements across the Company.
  • Participates in training opportunities to advance knowledge of drug development and Good Clinical Practice (GCP) guidelines.
  • Provides subject matter and drug development expertise as a key contributor to the medical strategy and execution of client programs.
  • Develops, reviews, and revises protocols, case report forms, training materials, project-specific tools, analysis plan designs, clinical trial reports, and new drug applications.
  • Provides medical and scientific expertise to project teams.
  • Acts as Medical Monitor/study support on a protocol or program basis for early clinical trials and is responsible for medical and safety monitoring on assigned projects.
  • Interacts with interdepartmental teams and external consultants as appropriate.
  • Participates in feasibility discussions relating to specific project proposals.
  • Participates in project risk assessment activities.
  • Assists, when needed, with Data Safety Monitoring Board activities.
  • Provides clinical and medical expertise to other Fortrea departments.
  • Contributes to the scientific and strategic leadership of a therapeutic area.
  • Performs other duties and responsibilities as assigned.

Required Qualifications
· MD or DO degree required.

  • Professional degree/designations/certifications/licenses legally required: MD/DO.
  • Relevant subspecialty fellowship training and history of board certification, as appropriate.
  • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
  • At least 10 years of experience; postgraduate training may be substituted by relevant expertise.
  • Recognized as a clinical research leader within their therapeutic area, with substantial knowledge of drug development and extensive clinical research experience within the pharmaceutical, biotechnology, CRO, or clinical research industry, which may be considered in lieu of board certification specialization where appropriate.

To be considered for this position, candidates must be legally authorized to work in the United States without the need for current or future employer-sponsored work authorization. Fortrea is unable to provide visa sponsorship or assume sponsorship of employment visas for this position.
Work Environment

  • Work is performed in an office environment with exposure to electrical office equipment.
  • Occasional domestic and international travel may be required.

Physical Requirements

  • Frequently stationary for 6 to 8 hours per day.
  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
  • Occasional crouching and stooping, with frequent bending and twisting of the upper body and neck.
  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
  • Light to moderate lifting and carrying (or otherwise moving) objects, including luggage and laptop computers, with a maximum lift of 15 to 20 pounds.
  • Regular and consistent attendance.
  • Varied hours may be required.
  • Pay Range
  • USD $173,000 - $320,000 annually
  • Benefits
  • All job offers will be based on a candidate's skills and prior relevant experience, applicable degrees/certifications, internal equity, and market data. Regular full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits, including Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), and Company bonus programs where applicable.
  • Application Deadline: September 28, 2026
  • Learn more about our EEO & Accommodations request here.

This job is curated by Lifelancer.
Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.
Please apply via Lifelancer platform to get connected to the application page and to find similar roles.
Originally posted on Himalayas

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