Senior Medical Director, Hematology/Oncology

IQVIA; Ciudad de México; Remote; MXN 3,323,000 - 4,431,000; Full time

Job summary

IQVIA is seeking a Senior Medical Director in Hematology/Oncology to provide strategic medical leadership across global clinical research programs. The role is home-based in the U.S.

or Canada and serves as Medical Monitor, interfacing with sponsors and investigative sites to ensure compliant, high-quality trial execution. You will guide protocol interpretation, safety assessment, medical data reviews, and urgent medical queries, while building a network of medical experts and supporting site

Qualifications

• MD degree from an accredited medical school.
• 5–7+ years of clinical practice as a licensed physician in Oncology/Hematology or related field.
• ≥3 years of clinical research experience as a study physician or in pharma/CRO/biotech.
• Board certification or eligibility in the relevant therapeutic area preferred.

Responsibilities

• Provide medical input to clinical programs including protocols, ICFs, and SAE evaluation.
• Oversee medical monitoring plans and review safety data across trials.
• Support site selection, investigator engagement, and patient recruitment strategies.
• Train study teams on protocol and therapeutic area.
• Review safety data and manage urgent medical queries to protect patient safety.
• Contribute to data interpretation and development of clinical study reports.
• Support proposal development and feasibility assessments for new business.
• Contribute to internal processes and quality improvement initiatives.

Skills

Advanced English

Clinical research experience

Medical monitoring / safety oversight

Education

MD degree from an accredited medical school

Job description

Job Posting Title- Senior Medical Director, Hematology/Oncology

Location: Home-based in the U.S. or Canada

Job Overview

The Senior Medical Director (Hematology/Oncology) is a strategic medical leader who provides scientific, clinical, and operational oversight across global clinical research programs. Acting as Medical Monitor, this role serves as the primary medical interface between IQVIA, sponsors, and investigative sites—ensuring high-quality, compliant, and efficient trial execution.

The role provides hands-on medical oversight, guiding protocol interpretation, eligibility, compliance, and safety, including medical data review and review of critical clinical data (e.g., alert laboratory results) and timely response to urgent medical queries to ensure patient safety and study continuity.

Essential Functions

• Provides medical and scientific input to clinical research programs including review of new business proposals, preclinical and/or clinical data, study protocols, training materials, informed consent, Investigator Drug Brochures, eCRFs, analysis plan designs, clinical study reports, regulatory approval submissions, serious and non-serious adverse event evaluation and reporting
• Ensures medical activities run according to GCP and operate with highest efficiency
• Establishes and maintains a network of medical/scientific consultants, etc.

Clinical Leadership & Study Execution

• Support site selection, investigator engagement, and patient recruitment/retention strategies
• Train study teams and investigators on protocol and therapeutic area
• Develop and oversee medical monitoring plans and serve as the primary medical resource for study teams and sites

Safety & Medical Oversight

• Ensure medical oversight of patient safety, including ongoing assessment of the study safety profile
• Review and interpret safety data, including SAEs and critical clinical data, ensuring accuracy and appropriate follow-up
• Support safety reporting activities and collaborate with sponsors and internal safety teams
• Manage unblinding procedures when required and contribute to regulatory interactions as needed

Data Review & Reporting

• Provide medical review of clinical data, including eCRFs, tables, and listings, to ensure accuracy and consistency
• Contribute to data interpretation and support development of clinical study reports

Business Development & Strategy

• Support proposal development, feasibility assessments, and client presentations
• Provide medical expertise to strengthen study design and strategic positioning in new business opportunities

Additional Contributions

• Support development of internal processes, training, and quality improvement initiatives
• Contribute to scientific literature review and medical input across projects as needed

Qualifications & Experience

• MD from an accredited, internationally recognized medical school
• 5–7+ years of clinical experience as a licensed physician within the relevant specialty (Oncology, Hematology, Surgical Oncology, or Urology with oncologic focus)
• Board certification or eligibility in the relevant therapeutic area strongly preferred or equivalent experience.
• Proven experience in clinical research (≥3 years) as a study physician/investigator or within Pharma, CRO, or Biotech environments.
• Advanced English level, able to speak and communicate fluently, able to discuss with different stakeholders about medical assessments for clinical trials. Global scope, global teams.

Key Competencies

• Strong ability to collaborate effectively within multidisciplinary and matrixed global teams, driving alignment and consensus
• Demonstrated ability to work independently while managing multiple priorities in a dynamic environment
• Excellent organizational skills with the ability to manage complex projects with shifting timelines and requirements
• Exceptional communication and interpersonal skills, with the ability to translate complex medical concepts into clear, actionable insights.

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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.