A renown pharmaceutical company spanning various established therapeutic areas in pharmaceutical industry and they are constantly growing with new product launches and innovations in contributing to the world.
Job Description
Maintain good relationships and interact with KOLs/ HCPs healthcare professionals and providers
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Cultivate and maintain relationships with key opinion leaders (KOLs), academic institutions, professional societies, and other external stakeholders.
Lead scientific exchange initiatives, including advisory boards, symposia, and educational programs, to disseminate clinical and scientific information about our products.
Collaborate with Medical Science Liaisons (MSLs) to identify and engage with KOLs and other healthcare professionals to gather insights and support evidence-based medicine.
To lead and coordinate in medical specialist recruitment and onboarding process.
Coordinate and participate in the clinical governance meetings including MDAC and Clinical Sub-Committees. Ensures that all MDAC, Subcommittees and clinical department meetings are held as per Terms of Reference.
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3. Assist in taking and distributing minutes of meeting and ensuring proper record keeping of minutes of meeting in the division. 4. Manage all documents in the division in a systematic filing system 5. Update and filing on relevant doctors practicing documents such as Annual Practicing Certificate, Doctor Practicing Certificate, CV, all doctors Agreements, legal letters, Indemnity Coverage, etc
6. Attend to calls and inquiries by doctors 7. Coordinate and arrange Continuing Medical Education (CME) activities for doctors including arrangement of venue & F&B, CPD points application, etc as relevant. 8. Ensure the credentialing & privileging of all new doctors are completed and in place upon start of practice and ensure the re-credentialing & re-privileging of all doctors are renewed timely prior to expiry
9. Assist on ad-hoc projects or assignment as and when needed
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A good basic degree from a reputable university Ability to collaborate across stakeholders. Strong organization and inter-personal skills are essential.
Proficient in Microsoft Office Good oral, written and presentation skills.
You will be involved in the Medical Affairs strategies, defining key scientific messages and will assume the key role as the interface between the healthcare industry and product development.
Duties will also include review of medical studies, publications, and clinical documents, developing relationships with KOLs and external organisations.
You will have the opportunity to exercise your scientific expert knowledge in the definition and implementation of new medical strategies.
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You will be involved in the Medical Affairs strategies, defining key scientific messages and will assume the key role as the interface between the healthcare industry and product development.
Duties will also include review of medical studies, publications, and clinical documents, developing relationships with KOLs and external organisations.
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Work closely with the other functions in the CRM TA Franchise team (e.g., marketing, MAHA and GTM).
Develop, implement, and execute strategies & activities to bring the benefit of BI medications to patients across the product lifecycle while collaborating and providing guidance to the OPUs.
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Deliver recurrent QI training and support via workshops and courses for a range of clinical and non-clinical staff where applicable.
Drive assigned quality improvement processes and programmes, from external and internal regulatory bodies, and co-develop change initiatives with clinical leads and participate in the shared learning while managing change within a complex team environment.
Identify new thinking and nurture new ideas from concept through pilot and into mainstream activity of emerging clinical and non-clinical topics relevant to clinical improvement and transformation.
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Within the Diagnostics Value & Medical Department, we are seeking a Medical Affairs Partner to provide medical and scientific support for our solutions with a core focus on cardiovascular & metabolic diseases. The Medical Affairs Partner is a field-based medical content expert in one or more therapeutic areas, responsible for developing and maintaining relationships with healthcare professionals (HCPs) in order to create a better understanding of products and increase disease/product awareness, providing clinical and scientific support for HCPs, and providing medical information for our products to patients, caregivers, and the general public. A bachelor’s degree or higher in a medical or life science discipline is typically required for this
position. The previous work experience must be in the pharmaceutical or medical device
Responsible for providing overall strategic and managerial leadership for the Medical Affairs function for the LOC, including strategic prioritization on projects and tasks in partnership with Takeda’s business stakeholders. He/she will contribute to the achievement of business success by putting the patient’s needs and safety into primary focus.
The Head of Medical Affairs will drive alignment across the Medical Affairs team, provide supervision for team members, and collaborate with key cross-functional stakeholders (e.g. compliance, marketing, commercial, and regulatory) across all Therapeutic Areas.
This position is responsible for planning and implementing medical strategies and tactics, to increase the understanding of Takeda products amongst healthcare professionals in the region.
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2. Oversees Doctors’ Accreditation and Credentialing, and Re-accreditation matters and to ensure that all doctors’ accreditation status is updated timely.
3. Manages medico-legal matters and Serious Reportable Events promptly and according to timeline.
1. Providing support to the Medical Advisory Board and Continuing Medical Education Committee.
2. Oversees Doctors’ Accreditation and Credentialing, and Re-accreditation matters and to ensure that all doctors’ accreditation status is updated timely.
3. Manages medico-legal matters and Serious Reportable Events promptly and according to timeline.
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Assess requirements for allocated product or product range to ensure complete regulatory compliance in the target region;
Liaise with both internal team and suppliers/manufacturers on regulatory issues and to obtain required documentation for regulatory compliance and new applications;
Prepare and lodge regulatory applications in relevant country;
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We are looking for a highly motivated Medical Affairs Director who is passionate about patient-centric HIV care, treatment, prevention, and Pre-exposure Prophylaxis (PrEP).
Candidate must be a self-starter with a proven track record of success in prior roles.
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2. Oversees Doctors’ Accreditation and Credentialing, and Re-accreditation matters and to ensure that all doctors’ accreditation status is updated timely.
3. Manages medico-legal matters and Serious Reportable Events promptly and according to timeline.