Clinical Development Medical Director - Cardiology

Healthcare Businesswomen’s Association; Greater London; Hybrid; GBP 100,000 - 125,000; Full time

Job summary

A leading global healthcare organization is seeking a Clinical Development Medical Director responsible for the scientific and clinical strategy of clinical trials. You will oversee data quality, manage cross-functional teams, and support regulatory compliance efforts. Ideal candidates should have an MD or equivalent, significant clinical practice experience, and a strong background in drug development. This role offers a hybrid work environment and the opportunity to impact patient care globally.

Qualifications

• 4+ years of clinical practice experience, including residency.
• 5+ years of experience in clinical research or drug development.
• 3+ years of conducting clinical trials in a global environment.

Responsibilities

• Provide clinical leadership and strategic input for clinical trials.
• Oversee medical and scientific review of trial data.
• Support safety reporting and ensure regulatory compliance.

Skills

Clinical Trials

Cross-Functional Teams

Data Analysis

Data Monitoring

Drug Development

Drug Discovery

Medical Research

Medical Strategy

People Management

Education

MD or equivalent medical degree

Medical Board certification

Job description

Job Description Summary

As a Clinical Development Medical Director, you will be responsible for the scientific and clinical strategy of assigned clinical trials, scientific monitoring, and reporting of quality data.

Job Description

#LI-Hybrid

Location: London UK, Barcelona Spain or Dublin, Ireland

Major accountabilities:

• Provide clinical leadership and medical strategic input for deliverables in the assigned project/program. Deliverables may include sections of individual protocols consistent with the clinical development plan (CDP), data review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications (e.g., investigator brochures, briefing books, safety updates, submission dossiers, and responses to health authorities)
• Drive execution of the section of the program in partnership with global line functions, assigned Global Trial Directors, and regional/country medical associates
• Oversee/conduct medical and scientific review of trial data with Clinical Scientific Expert (CSE). May be the Program Manager of other associates (e.g.., CSE). May function as study medical monitor
• Support GPCH in ensuring overall safety of the molecule. May be a core member of the Safety Management Team, and supports program safety reporting (e.g., PSURs, DSURs, and safety related documents) in collaboration with Patient Safety
• Support the Clinical Development Head by providing medical input into CDP and clinical trial package reviews and contributing/driving development of disease clinical standards for disease areas
• Provide support to the GPCH or CDH in interactions with external partners (e.g., regulatory authorities, key opinion leaders, data monitoring boards, advisory boards, patient advocacy groups), internal partners (e.g., clinical trial team, Medical Affairs, Commercial, Health Economics & Outcomes Research), and decision boards
• Work with BR (Novartis Biomedical Research)/Translational Medicine) to drive transition of early development projects to Transition Decision Point and with Business Development, including target identification and due diligences
• Ensure career development of Program Reports and clinical colleagues through active participation in performance management and talent planning processes. Provide on-boarding, training, & mentoring support
• Contribute to medical/scientific training of relevant Novartis stakeholders on the disease area and compound/molecule. May serve as speaker for Global Clinical team

Minimum Requirements:

• MD (or equivalent medical degree) required. Training in cardiology preferred
• Medical Board certification preferred. 4+ years Clinical practice experience (including residency) preferred
• Possess advanced knowledge and clinical training in a medical/scientific area (e.g., internal medicine or sub-specialty) required
• 5+ years of experience in clinical research or drug development from the pharmaceutical/biotechnology industry, preferably spanning clinical activities in phases I through IV
• 3+ years of contribution to and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting, and publishing) in a global/matrixed environment
• Showcase advanced knowledge of assigned therapeutic area
• Demonstrate ability to establish strong scientific partnership with key partners
• Need thorough knowledge of Good Clinical Practice, clinical trial design, statistical analysis methodology, and regulatory/clinical development processes
• People management experience preferred, especially at the global level (this may include management in a matrixed environment)

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Accessibility and accommodation

Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [e-mail] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Skills Desired

Clinical Trials, Cross-Functional Teams, Data Analysis, Data Monitoring, Drug Development, Drug Discovery, Medical Research, Medical Strategy, People Management