Medical Director

IQVIA Inc; Pasig; On-site; PHP 900,000 - 1,200,000; Full time

Job summary

IQVIA Inc. is seeking a Medical Director to lead medical and scientific leadership across global clinical research programs. In this role, you will partner with project teams, investigators, and clients to support protocol execution, participant safety, and scientific excellence.

This role includes medical monitoring responsibilities and strategic medical input to business development activities, proposal development, and study design, helping to shape innovative solutions for our clients.

Qualifications

• Medical degree required and license to practice medicine.
• Minimum 5 years of clinical practice and 5–7 years in clinical medicine/research.
• Experience in pharma/CRO/biotech environments preferred.

Responsibilities

• Serve as Global/Regional Medical Advisor on clinical research projects.
• Provide medical and scientific guidance to project teams and investigators.
• Review study protocols, CRFs, and safety data; support SAE assessments.
• Deliver therapeutic area training and participate in investigator and client meetings.
• Contribute to AOSE, CSR reviews, and medical safety evaluations.

Skills

Medical leadership

Clinical research

Strategic thinking

Communication

Project collaboration

Travel readiness

Education

Medical degree from accredited school

Job description

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 periodicl on a regional and international basis.

About IQVIA

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.

Integrity Statement

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.

Culture and Values

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Closing

Thank you for your interest in growing your career with us.