Medical Science Liaison (Cell Therapy) Supervisor

Pengiklan Anonim; Jakarta Selatan; On-site; IDR 600,000,000 - 900,000,000; Full time

Job summary

Pengiklan Anonim seeks an experienced Medical Science Liaison (Cell Therapy) Supervisor in South Jakarta to lead the MSL team, manage key physician relationships, and oversee evidence generation for cell therapy products. The role emphasizes scientific integrity, collaboration with PV, and driving publications and studies.

The successful candidate will have at least 2 years in Medical Affairs or similar, with strong capability to translate complex data into actionable insights for internal

Qualifications

• Bachelor’s degree or higher in Pharmacy, Medicine, Life Sciences, Biotechnology, or related field.
• At least 2 years in Medical Affairs/Medical Science Liaison or related roles within pharma/biopharma/ATMP.
• Experience related to cell therapy, biologics, orthopaedics, dermatology, neurology, or regenerative medicine.
• Proven ability to lead scientific exchange with physicians and KOLs with balanced, evidence-based discussions.

Responsibilities

• Lead scientific exchange & medical education for physicians and healthcare teams.
• Generate and capture Real World Evidence (RWE) insights and translate into internal reports.
• Lead investigator-led or company-supported evidence generation initiatives.
• Develop and manage a KOL network focused on clinical evidence and scientific advocacy.
• Ensure medical governance, safety culture, and cross-functional collaboration.

Skills

Scientific exchange

KOL development

Field leadership

Stakeholder management

Medical affairs

Education

Bachelor’s degree in Pharmacy/Medicine/Life Sciences

Advanced degree (MSc/PharmD/MD/PhD)

Job description

Medical Science Liaison (Cell Therapy) Supervisor

About the role
Our Client is seeking an experienced and dynamic Medical Science Liaison (Cell Therapy) Supervisor to join our Clinical/Medical Research division. This is a full-time position based in South Jakarta, Jakarta, where you will play a pivotal role in leading our medical science liaison team within the cell therapy space. As supervisor, you will be responsible for managing a team of medical science liaisons whilst maintaining your own strategic relationships with key healthcare professionals and opinion leaders. This role is essential to ensuring the successful dissemination of scientific evidence and supporting healthcare providers in delivering advanced cell therapy treatments to patients.

Key responsibilities

• 1. Scientific Exchange & Medical Education
  - Lead scientific discussions with physicians and healthcare teams on mechanism of action, clinical rationale, patient selection, administration considerations, and safety monitoring for stem cell and its derivatives products.
  - Deliver ongoing education through scientific visits, journal reviews, slide sessions, and clinical literature updates, tailored by specialty (orthopaedics, dermatology, neurology, fertility, etc.).
  - Serve as the internal “go-to” for clinical/scientific questions from the field, ensuring responses are accurate, consistent, and evidence-based.
• 2. Insight Generation: Scientific Feedback & Evidence Capture (Real World Evidence/RWE)
  - Systematically collect medical insights from doctors after product use (effectiveness signals, protocol variations, patient selection, outcomes, limitations, practical barriers).
  - Convert field learnings into structured outputs (e.g., insight reports, RWE summaries, case documentation packages) that can support internal decision-making.
  - Identify unmet needs and emerging clinical trends to guide evidence priorities (what data is missing, what endpoints matter to doctors, what protocols are realistic).
• 3. Research Collaboration Leadership (Investigator-Led & Company-Supported Evidence)
  - Proactively identify and develop research opportunities with KOLs (case series, observational studies, registries, small mechanistic studies).
  - Lead scientific alignment discussions with investigators: research question, study design concept, inclusion/exclusion, endpoints, follow-up schedule, data elements, and publication plan.
• 4. KOL Development & Scientific Network Management
  - Build, map influence pathways, and maintain a KOL network focused on clinical evidence generation and scientific advocacy.
  - Facilitate peer-to-peer scientific exchange (case sharing meetings, advisory boards, clinical roundtables) and ensure discussion outputs are documented and actioned.
• 5. Medical Governance, Safety Culture & Cross-functional Bridge
  - Act as the scientific bridge between field and internal stakeholders by translating clinical feedback into actionable recommendations for: training needs, protocol standardization, message refinement, and evidence gaps.
  - Partner with PV by ensuring field feedback includes safety signals and encouraging appropriate AE awareness/reporting (without replacing PV’s formal process).
  - Support internal readiness by reviewing/creating scientific field materials (FAQs, slide decks, scientific response letters) aligned with evidence and compliant communication standards.
• 6. Internal Capability Building (Scientific Enablement)
  - Train commercial/field teams on core scientific narratives (what we know, what we don’t know, proper claims boundaries) so doctor communication stays credible and consistent.
  - Provide scientific input for new product/channel readiness: key evidence, anticipated objections, discussion pathways by specialty, and scientific differentiation vs competitors.

What we're looking for

Bachelor’s degree or higher in Pharmacy, Medicine, Life Sciences, Biotechnology, or a related field; advanced degree (MSc/PharmD/MD/PhD) is a plus, with strong ability to interpret clinical and scientific literature.

At least 2 years of experience in Medical Affairs/Medical Science Liaison, clinical research, or scientific field roles within pharma/biopharma/ATMP, preferably related to cell therapy, biologics, orthopaedics, dermatology, neurology, or regenerative medicine.

Proven capability to lead high-quality scientific exchange with physicians and KOLs, including discussing mechanism of action, clinical rationale, patient selection, administration considerations, and safety monitoring in a balanced, evidence-based manner.

Demonstrated experience in collecting and synthesizing field medical insights (post-use feedback, outcomes, protocol variations, unmet needs, and safety signals) and translating them into structured internal reports that guide strategy, education, and evidence generation priorities.

Experience supporting or initiating evidence generation activities (e.g., case series, observational studies, registries, investigator-led research), including ability to align with investigators on study concepts, endpoints, data elements.

Excellent communication, stakeholder management, and collaboration skills, with the ability to work effectively across marketing/sales/clinical teams while maintaining medical governance and compliance standards.

What we offer

Our client is committed to supporting the professional growth and well-being of their employees. They offer a competitive compensation package including performance bonuses, comprehensive health insurance coverage, and opportunities for ongoing professional development through training and conference attendance. We recognise the importance of work-life balance and provide flexible working arrangements where feasible. Our Client collaborative culture emphasises innovation, scientific integrity, and making a meaningful impact in advancing patient care through cell therapy. They encourage a supportive work environment where team members can thrive and contribute their expertise to cutting-edge medical research and development.

About us

Our Client is a forward-thinking healthcare and medical research organisation dedicated to advancing clinical and medical innovation. Specialising in the cell therapy sector, we partner with healthcare institutions, clinicians, and researchers to bring transformative treatments to patients. Our mission is to bridge the gap between scientific discovery and clinical application by providing expert medical science liaison services and comprehensive scientific support. With a commitment to regulatory compliance, scientific excellence, and patient-centred care, Our Client is recognised as a trusted partner in the global cell therapy landscape. We foster an environment of collaboration, continuous learning, and scientific integrity, where our team members are empowered to make a real difference in advancing healthcare innovation.