Associate Clinical Development Medical Director (Inmarket Brands)

Novartis; London; On-site; GBP 90,000 - 120,000; Full time

Job summary

A leading pharmaceutical company is seeking an Associate Clinical Development Medical Director to oversee clinical trials and ensure data quality. The role involves significant medical oversight, contributing to trial documentation, and mentoring clinical development associates. Ideal candidates will have an MD, extensive clinical experience, and a strong background in clinical research.

Qualifications

• Clinical practice experience ≥ 4 years preferred.
• Working knowledge of GCP, clinical trial design, statistics.

Responsibilities

• Provides clinical oversight and medical input for clinical trials.
• Ensures direct medical oversight and support of trials.
• Contributes to trial-related documents and regulatory submissions.

Skills

Budget Management

Clinical Research

Coaching

Data Analysis

Risk Management

Education

MD or equivalent medical degree

Job description

Job Description Summary
The Associate Clinical Development Medical Director (Assoc. CDMD) is responsible for the scientific and medical oversight of assigned clinical trial(s), medical, safety and data monitoring, and reporting of quality data. May be responsible for the scientific and medical strategy of assigned sections of a clinical development program, depending on the size and complexity.

Job Description

Major accountabilities:

• Provides clinical oversight, medical and scientific input, and contributes to development of trial related documents (e.g., CTPs, informed consent form, case report forms, data monitoring committee charters, data analysis plan, reports, publications) for assigned clinical trial(s) consistent with Integrated Development Plan (IDP) and Clinical Development Plan (CDP); develops materials for trial-related advisory boards, data monitoring committees, investigators meetings, and protocol training meetings for Novartis local medical organizations
• Provides medical and scientific input and contributes to clinical sections of trial and program level regulatory documents (e.g., Investigator's Brochures, Health Authority briefing books, safety updates, submission dossiers, and responses to Health Authorities)
• In collaboration with appropriate Clinical Trial Team (CTT) members:
• Ensures direct medical oversight and support of trials as needed and acts as the medical monitor which includes data, safety and medical scientific review of all clinical trial documents and data
• Conducts ongoing medical and scientific review of clinical trial data with support of Clinical Scientific Expert(s) and CDDs
• Manages patient safety and reports on trial data to safety and clinical boards (e.g., Safety Management Team (SMT), GCT, GPT) under leadership of the Sr CDMD or GPCH
• Provides input into final analyses and interpretation including the development of the Clinical Study Report(s) (CSRs), publications and internal/external presentations, with appropriate oversight from Medical Lead
• Under the direction of the GPCH or (Sr.) CDMD, supports assessment of overall benefit/risk assessment and monitor safety of the molecule for the assigned section on an ongoing basis and may be a member of the Safety Management Team (SMT), and supports overall program safety reporting (e.g., Periodic Safety Update Reports (PSURs), Drug Safety Update Reports (DSURs), and other safety related documents) in collaboration with Patient Safety
• Contributes to talent and career development of CD associates through on-boarding, coaching, and/or mentoring support; develops and fosters CD culture; and may contribute to the performance evaluation of CTT members
• Contributes to medical/scientific training of relevant Novartis stakeholders on the disease area and compound/molecule. May serve as speaker for franchise medical/scientific training

Minimum Requirements:

• MD or equivalent medical degree required.
• Advanced knowledge and clinical training in a medical/scientific area (e.g., pediatrics, internal medicine or sub-specialty) preferred, with Medical Board certification preferred;
• Clinical practice experience ≥ 4 years (including residency) preferred

Work Experience:

• ≥ 3 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV.
• ≥ 2 years of contribution to and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing) in a global/matrix environment in pharmaceutical industry
• Working knowledge of the assigned disease area is desired with proven ability to interpret, discuss and present efficacy and safety data relating to clinical trial(s) or program level
• Demonstrated ability to establish effective working relationship with stakeholders
• Working knowledge of GCP, clinical trial design, statistics, and regulatory and clinical development processes

Why Novartis? Our purpose is to reimagine medicine to improve and extend people's lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture

You'll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network

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Skills Desired
Budget Management, Clinical Research, Clinical Trial Protocol, Clinical Trials, Coaching, Cross-Functional Teams, Data Analysis, Learning Design, Lifesciences, Risk Management, Risk Monitoring