Kelly Services is currently seeking Medical Directors and Sr Medical Directors for long-term engagements or possible permanent opportunities with one of our Global Pharmaceutical clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vison, 401K, and a variety of other benefits to choose from. You may also be eligible for paid time off, including holiday, vacation, and sick/personal time.
The Senior Medical Director Marketed Products (SMDMP) is accountable for Medical Sponsor and Clinical oversight for assigned marketed products globally, and contributes to new business evaluation of marketed products. Usually responsible for multiple products and at least one complex product.
The SMDMP is an integral member of a R&D Marketed Product Team (R&D MPT) that is responsible for providing dedicated R&D support for the products under its purview. The MDMP interacts and partners with marketed products R&D function leads (regulatory affairs, pharmacovigilance, global development operations and project management) to set R&D strategy and prioritise R&D functional support for assigned MP portfolio. This individual is responsible for medical and clinical scientific leadership for the assigned R&D Marketed Product Team (R&D MPT) and product specific global program teams (GPT) or established product teams (EPT) as required,
The SMDMP provides Medical Sponsor Oversight for all products managed by the R&D MPT as part of the dedicated, integrated R&D support to ensure the ability to meet its corporate obligations as MAH for assigned products. The MDMP provides medical and clinical leadership to make sure that the R&D MPT anticipates potential compliance risks, and has appropriate contingency plans in place to allow the rapid response to regulatory agency, scientific, or commercial hurdles.
The SMDMP will be required to be the medical and clinical scientific expert for the assigned products and to develop and maintain an up-to-date expert knowledge of the scientific, medical and regulatory aspects of the products in order to provide medical, clinical and scientific support, guidance, mentoring and leadership across these areas.
Partner with R&D Marketed Product Project Manager to coordinate R&D function support for assigned products within the R&D MPT. Provide medical and clinical scientific leadership and expertise for assigned products to support other R&D function leads within the R&D MPT.
Establish integrated partnership(s) with R&D functional leads on assigned R&D MPT (regulatory affairs, pharmacovigilance, global development operations).
Collaborates with the commercial organization and Established Products Teams and Sub Teams. Also works directly with LOCs when required
Form integrated partnerships and collaborate with all relevant cross-divisional stakeholders involved in the support of assigned products, including but not limited to, Quality, Global Manufacturing and Supply, Medical Affairs (Global and Regional), Global Commercial, LOC MDs, Regional Business Units (e.g., product brand leads) and LOC product leads.
Forms integrated partnerships with and works with Global Product Team Leaders (GPL) and Established Product Team Lead (EPTL) as necessary, and ensures excellence in delivery of medical and clinical support and execution of clinical development activities/studies across assigned products. Ensure the R&D MPT works effectively to support GPT/EPTs.
Forms integrated partnership with strategic partner vendor(s) and provide oversight of all strategic partner vendor medical and clinical deliverables for all products in assigned R&D MPT. Ensure highest quality of medical/clinical science input and clinical components of deliverables from the strategic partner vendor.
Sponsor supervision and guidance for vendor medical monitors
Partners with strategic partner vendor(s) and drives medical and clinical scientific activities relating to the preparation / approval of protocols and the conduct of clinical studies to support LCM, post marketing requirements and regional or local registration as needed. Provides client oversight of strategic partner MDs/clinical staff involved in these activities. Accountable for the successful design, execution and interpretation of clinical studies.
Oversees the strategic partner vendor(s) to ensure appropriate and continuous medical monitoring and medical data review of clinical studies, protecting the safety of patients within the study. Responsible for internal oversight of strategic partner vendor medical monitoring activities, assessing issues related to protocol conduct and/or individual subject safety. Assesses overall safety information for studies and compound in conjunction with Pharmacovigilance. Makes final decisions regarding study conduct related to scientific integrity
Establish integrated partnership with strategic partner clinical operations and statistical functional leads to ensure the integrity and correctness of data analysis and interpretation with the appropriate integration of safety and efficacy data from clinical studies longitudinally and cross-sectionally in support of regulatory submissions, ensuring data quality and adherence to national and international regulations and requirements and ICH.
Participates in cross functional non-project-specific initiatives and committees on behalf of project clinical perspective as well as general clinical science functional perspective
Presents study conclusions to management and determine how individual study results impact the product strategy. Interprets data from an overall scientific and regulatory standpoint as well as within the context of the medical significance to individual patients
Participate in and support all required regulatory submissions/interactions for assigned products. Represent the client as Responsible Medical Doctor and Medical/Clinical expert to regulatory agencies globally for assigned products as needed. Support Local Operating Company (LOC) medical staff for all regulatory agency interactions as needed. Drive medical and clinical scientific input and development of required documents for regulatory applications/submissions (e.g. briefing reports, CTDs, IND updates, PSUR updates, label changes etc.), materials used for meeting presentations, and formal responses to communications received from the regulatory agencies.
Provide scientific education and mentoring for internal and external audiences (academic partners, scientific community, regulatory agencies)
Oversee compliance with internal SOPs and external legal requirements, including training of personnel, contractual arrangements with external service providers and partner companies.
Build and develop medical and clinical expert relationships to ensure delivery and maintenance of state-of-the-art medical therapeutic and clinical scientific expertise into medical and clinical R&D support for assigned marketed products Due Diligence, Business Development & Alliance Projects
Participate, conduct and oversee clinical due diligence evaluations and development of clinical development plans for potential alliances and or in-licensing opportunities.
Assess both scientific and development feasibility, evaluating strategic fit with overall portfolio, evaluating complete or ongoing clinical trials, assessing regulatory interactions and future development plans, interacting with upper management of potential partner/acquisition companies during due diligence visits and alliance negotiations, and actively participating on internal assessment teams in conjunction with commercial colleagues.
REQUIRED EDUCATION, LICENSES/CERTIFICATIONS:
MD or internationally recognized equivalent plus 8 years of clinical research experience within the pharmaceutical industry, CRO health-related consulting company, or biomedical/clinical experience within academia (or a combination of afore mentioned).
Participation in NDA/MAA/Submission experience
Track record and demonstrated ability to lead and manage both science and business aspects of drug development.
Experience with and demonstrated ability to lead and manage highly trained medical, scientific and technical professionals
Superior communication, strategic, interpersonal and negotiating skills
Ability to proactively predict issues and solve problems
Ability to drive decision-making within a multi-disciplinary, multi-regional, matrix teams
Diplomacy and positive influencing abilities across multinational business cultures
Emerging research in Translational Medicine
Nonclinical and clinical drug discovery and development
TMS state-of-the-art technologies
Regional/global Regulatory requirements
Kelly® Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interests-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.
At Kelly, we're always thinking about what's next and advising job seekers on new ways of working to reach their full potential. In fact, we're a leading advocate for temporary/nontraditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live (plus, did we mention we provide a ton of benefits?). Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.
Kelly is an equal opportunity employer committed to employing a diverse workforce, including, but not limited to, minorities, females, individuals with disabilities, protected veterans, sexual orientation, gender identity. Equal Employment Opportunity is The Law.