Company Description
docfliq is a medical knowledge and medico-marketing company partnering with global pharma medical affairs teams across MEA, Europe, APAC, and LatAm. We design and deliver Delphi consensus programs, KAP studies, real-world evidence, accredited HCP education, and capacity-building suites across therapy areas including vaccines, cardiovascular rare disease, hematology, neurology, oncology, IBD, and infectious disease. Our clients are leading global innovative pharma companies. With offices in Dubai, Singapore, and India, docfliq sits at the intersection of scientific rigor, editorial craft, and AI-enabled HCP engagement.
Role Description
This is a senior, full-time role based in Dubai (UAE residents) or Mumbai, hybrid with 2 to 3 days in office. Fully remote considered for exceptional candidates.
The Senior Manager, Medical Affairs will lead scientific strategy and narrative across 4 to 6 concurrent client programs. Responsibilities include shaping the scientific story arc for Delphi consensus programs, KAP studies, advisory boards, and accredited HCP certification programs. The role involves writing and owning HCP-grade content end to end, including scientific decks, accredited learning modules, expert briefing documents, and manuscript-style deliverables.
The candidate will partner directly with pharma medical affairs counterparts at affiliate, regional, and global level, and will hold scientific discussions with KOLs and internal medical leads. They will translate clinical evidence into stories that move HCPs, working alongside the design team to ensure the science survives the journey from manuscript to slide.
This is a peer seat on a senior team. Work ships under the candidate's name.
The candidate will also help shape the scientific layer of docfliq 2.0, our next-generation AI-enabled platform for HCP medical education, currently in build.
Qualifications
Clinical or life sciences foundation (MD, MBBS, PharmD, PhD, or equivalent depth)
5+ years in pharma medical affairs, MSL leadership, or a tier-1 medical communications agency working on global or regional pharma accounts. Years flexible for exceptional candidates
Genuine command of at least one major therapy area, with the ability to debate trial design, not just summarise it
Proven portfolio of scientific narrative work, including decks, advisory board reports, accredited modules, or publications
Excellent written English. This role is approximately 60 percent writing
Comfort working with global pharma stakeholders across time zones
Maturity to navigate sensitive client conversations
Good to have
HEOR or evidence generation exposure (burden of disease, value dossiers, RWE protocols)
Slide craft and visual storytelling instincts
Experience with accredited learning frameworks (CME, CPD, SCFHS, EACCME, RCP, UCL, or similar)
Working knowledge of MEA, Europe, APAC, or LatAm pharma markets
Seniority Level
Head level. Open to Director for exceptional candidates.
How to Apply
Send your CV along with 2 to 3 work samples (decks, modules, advisory board reports, or publications you led the scientific narrative on) to , with and in copy.
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