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Open nowFirst seen 2 hours ago

Medical Director

Lifelancer3,904 open roles

Where
Remote
Work mode
Remote
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Your applicationOpen nowMedical DirectorLifelancer · Remote

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The clock on this job

Early applications get read.

12.9% of postings close within 7 days. Measured by our own scanner across the market. Lifelancer postings stay open a median of 5 days.

Share of postings closed within
  1. 2.2%1 day
  2. 4.7%3 days
  3. 12.9%7 days
  4. 21.0%14 days
  5. 35.6%30 days
  6. 58.5%60 days
This job: first seen 2 hours ago

Lifelancer median: 5 days open

The posting

Job Title: Medical Director

Job Location: Mumbai, Maharashtra, India

Job Location Type: Remote

Job Contract Type: Full-time

Job Seniority Level:

IQVIA is seeking a Medical Director to join our Medical Services team and provide medical, clinical, and scientific leadership across global and regional clinical research programs. In this role, you will serve as a key medical expert throughout the clinical trial lifecycle, partnering with project teams, investigators, and clients to support protocol execution, participant safety, and scientific excellence. In addition to medical monitoring responsibilities, you will contribute strategic medical insight to business development activities, proposal development, and study design, helping to shape innovative solutions for our clients.

Responsibilities:

  • Primarily serve as the Global and/or Regional Medical Advisor on assigned clinical research projects.
  • Serves as Scientific Advisor and provides medical and scientific guidance to project teams, ensuring the highest standards of patient safety, protocol compliance, and scientific integrity.
  • Act as a trusted medical expert for investigative sites and study teams, supporting protocol interpretation, inclusion/exclusion determinations, patient eligibility assessments, and safety-related matters.
  • Review and provide medical input into study protocols, Investigational Brochures, Case Report Forms (CRFs), and other key study documentation.
  • Deliver therapeutic area and indication-specific training to clinical project teams.
  • Attend and present at Investigator Meetings, client meetings, and other study-related forums.
  • Perform medical review and clarification of trial-related Adverse Events (AEs) and support Serious Adverse Event (SAE) assessment in collaboration with Pharmacovigilance teams.
  • Contribute to Analysis of Similar Events (AOSE), adverse event coding reviews, and other medical safety evaluations as required.
  • Review Clinical Study Reports (CSRs), patient narratives, and other clinical study deliverables.
  • Provide timely medical support for protocol-related questions from investigative sites throughout the course of a study.
  • Support the development of medically sound study delivery strategies for regional and global clinical trials.
  • Partner with Business Development and operational teams to provide medical and scientific expertise during proposal development, feasibility assessments, and bid defense meetings.
  • Advise on therapeutic landscapes, standard of care, patient recruitment strategies, investigator identification, and competitive market considerations.
  • Participate in client presentations, strategic business development activities, and scientific discussions with external stakeholders.
  • Maintain awareness of emerging scientific, clinical, and regulatory developments within relevant therapeutic areas.
  • Maintain awareness of industry development and contribute to scientific publications as appropriate.

Qualifications:

  • Medical degree from an accredited and internationally recognized medical school.
  • Current or previous license to practice medicine.
  • A minimum of 5 years of clinical practice experience following medical qualification.
  • 5-7 years of relevant experience in clinical medicine and clinical research, including experience within the pharmaceutical, biotechnology, CRO, or healthcare industry.
  • Previous clinical research experience as an investigator or in the Pharma, CRO or Biotech industry is required.
  • Strong understanding of clinical trial methodology, drug development processes, and applicable regulatory requirements.
  • Current knowledge of the scientific, clinical, regulatory, and competitive landscape within relevant therapeutic areas.
  • Specialty Board certification in a relevant therapeutic area is preferred.
  • Demonstrated ability to provide expert medical consultation and scientific guidance across multiple projects and stakeholders.
  • Strong communication, presentation, and interpersonal skills, with the ability to engage effectively with clients, investigators, and cross-functional teams.
  • Ability to establish and maintain effective working relationships with colleagues, sponsors, and external partners.
  • Willingness to travel periodically on a regional and international basis.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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.

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