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高级医学总监,风湿病学 - 美国远程

Sr. Medical Director, Rheumatology - US Remote

其他限定地区(需当地身份)
公司Lifelancer
薪资$240,000 - $340,000/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15 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:高级风湿病医学总监 - 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:

高级风湿病医学总监 - 美国远程办公

提升CRO标准,推动创新和交付,帮助更快地将改变生命的治疗方案带给患者。Fortrea正在寻找一位具有深厚风湿病学专业知识以及创新疗法(包括细胞和基因疗法)背景的美国远程办公医学总监或高级医学总监。该职位将为所有开发阶段提供医学领导和监督,包括早期创新和后期全球项目。负责支持其专业领域内拟议和正在进行的项目的开发活动,以及对指定临床研究的医学监测。

(高级)医学总监将在客户互动、商务拓展讨论和提案展示中担任关键医学代表。该职位还将促进并加强与全球临床运营团队的关系,并作为I-IV期临床试验的首席医学专家提供领导力。

我们特别关注那些曾主导或支持过风湿病临床项目的候选人,他们能够胜任研究医生的角色,提供医学监测监督(例如安全性审查、参与方案制定,包括研究设计、终点和入选标准),并与项目组其他成员协作。除了强大的科学领导能力,该职位还需要高度面向客户,具备更强的商务拓展成分——需要定期与高管层进行交流,并具备自信和专业素养,以代表Fortrea与高级客户领导、外部合作伙伴和其他关键利益相关者进行沟通。

您将负责:

  • 高水平的医学技术评估和临床试验主题专家(SME)贡献(可能是区域或全球范围)。
  • 与客户医学团队、项目团队、关键意见领袖以及主要研究者/机构层面进行跨职能、科学和技术方面的SME贡献和互动。
  • 与客户和内部团队合作,支持商务拓展——塑造临床/医学策略,用于提案、投标答辩和客户讨论。
  • 对医学监测活动进行监督,确保医学交付物的时间节点和质量。
查看英文原文

Job Title: Sr. Medical Director, Rheumatology - US Remote
Job Location: Durham
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:

Senior Medical Director, Rheumatology - US Remote Based

Raising CRO standards for innovation and delivery to help bring life-changing treatments to patients faster. Fortrea is seeking a dedicated US remote basedMedical Director or Senior Medical Director with deep expertise in Rheumatology along with background in innovative therapies, including cell and gene therapy.  The incumbent will provide medical leadership and oversight across all phases of development, including early-phase innovation and late-phase global programs. Responsible for supporting the development activities of proposed and ongoing projects in their area of expertise, as well as medical monitoring to assigned clinical studies.

The (Senior) Medical Director will serve as a key medical representative in client interactions, business‑development discussions, and proposal presentations. The role will further foster and enhance relationships with global clinical operations teams and provide leadership as the Leading Physician for Phase I–IV clinical trials).

We are particularly interested in candidates who have led or supported rheumatology clinical programs and who are comfortable serving as the study physician, providing medical monitoring oversight (e.g., safety review, contribution to protocol development, including study design, endpoints and eligibility criteria) and working collaboratively with other project team members. In addition to strong scientific leadership, the role is expected to be highly client-facing with an increased business development component - requiring regular engagement at executive level, and the confidence and polish to represent Fortrea with senior client leaders, external partners, and other key stakeholders.

WHAT YOU WILL DO

  • High level Medical TA and Clinical Trial Subject Matter Expertise (SME) contributions (may be Regional or Global).
  • SME Cross-functional, scientific & technical contributions and interactions with Clients Medical teams, Project teams, Key Opinion Leaders and at Principal Investigator/Site levels.
  • Partner with clients and internal teams to support business development - shaping clinical/medical strategy for proposals, bid defences, and client discussions.
  • Provide oversight of medical monitoring activities to ensure timelines and quality of medical deliverables and assigns physician resources as required.
  • According to the scope of work, may serve as Global Lead, Regional or Program Project Physician across multiple indications.
  • Provide subject matter and drug development expertise and is a key contributor to the medical strategy and execution of the study/program for the client.
  • Provides input, review and revision of protocols, case report forms, training materials, project specific tools, analysis plans design, clinical trial reports and new drug applications.
  • Prepares materials for and actively participates in investigator meetings and assists at site initiation visits.
  • Provides medical/scientific expertise to project team.
  • And any other duties as required or assigned.

YOU NEED TO BRING…

Qualifications (Minimum Required and preferred):

  • MD Degree
  • Board Certification in Internal Medicine
  • Specialization in Rheumatology and broader therapeutic experience in autoimmune diseases (AID)
  • Preferred: Specific expertise in cell and gene therapy in autoimmune diseases (AID)
  • 3+ years of substantial knowledge of drug development and extensive clinical research experience within the pharmaceutical/CRO industry (or as a clinical trial investigator)
  • Preferred: Industry experience inclusive of clinical trials medical monitoring experience or other relevant clinical development/trial experience at a CRO, pharmaceutical company, regulatory agency
  • Strong scientific communication and client‑facing capabilities, including presenting scientific expertise, supporting proposals, and strengthening external partnerships
  • English language skills: Full professional proficiency

Work Environment

  • Remote position based in USA
  • Occasional national and international travel required, including attendance at sponsor meetings, investigator meetings, and relevant scientific or industry conferences.

Physical Requirements

  • Frequently stationary for 6-8 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, stooping, with frequent bending and twisting of 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 moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
  • Regular and consistent attendance.
  • Varied hours may be required.

Pay Range: USD $240,000-$340,000

Benefits: All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as 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), Company bonus where applicable.

Application Deadline: August 30, 2026

#remote

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.
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Originally posted on Himalayas

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