Associate Project Specialist – Medical Communications

HYDERABAD (IN)HYBRIDPOSTED: 9/29/2026
PHARMAFull time
HIRING ORGANIZATIONSANOFIPharmaceuticals / Biotechnology
Sanofi

ROLE OVERVIEW

Sanofi Business Operations (SBO) in Hyderabad is the strategic engine behind the company's global medical and scientific communications, serving Specialty Care, Vaccines, General Medicines, Consumer Healthcare, CMO and R&D. This Associate Project Specialist role sits at the intersection of project management and medical communications, coordinating the end-to-end delivery of publications, slide decks, abstracts, posters and manuscripts produced by scientific writers. Because these deliverables carry Sanofi's scientific voice into journals, congresses and regulatory conversations, flawless planning, compliance and stakeholder choreography are mission-critical. Working inside a global capability hub gives the post-holder rare exposure to therapeutic-area science, publication governance platforms such as iEnvision and PromoMats, and senior medical stakeholders across geographies — a strong launchpad for a career in medical writing, publications management or medical affairs operations.

ROLE DEFINITION & RESPONSIBILITIES

  • •Coordinate end-to-end project management support for assigned publications and medical education deliverables, from initiation and amendment through final approval and archival.
  • •Track submission timelines, milestones, risks and issues on iEnvision, escalating blockers to Project Managers and scientific writers proactively.
  • •Route documents through compliance and approval platforms such as PromoMats and NAYA, ensuring version control and audit-ready documentation.
  • •Draft, initiate and amend submissions based on reviewer comments, incorporating feedback from internal and external stakeholders accurately.
  • •Monitor allocated budgets and external spend, processing purchase orders, goods-received notes and vendor invoices with finance partners.
  • •Maintain regular communication with global scientific communication and medical content enhancement teams to align on scope, quality and timelines.
  • •Ensure slide decks, abstracts, posters and manuscripts are delivered, stored and versioned per agreed quality standards.
  • •Contribute to continuous process improvement by adopting new tools and technologies that raise productivity and scientific quality.

QUALIFICATIONS & REQUIREMENTS

REQUIRED QUALIFICATIONS

  • University graduate degree, preferably in life sciences, pharmacy, biotechnology or a related scientific discipline.
  • Postgraduate qualification (M.Pharm, MSc, PharmD or similar) in life sciences is strongly desirable.
  • 2–4 years of post-qualification experience in medical communications, scientific writing support or publication management.
  • Prior experience in a pharmaceutical company, CRO, medical communications agency or healthcare capability centre.
  • Demonstrated exposure to publication planning processes and compliance or approval workflows.
  • Excellent spoken and written English, with the ability to communicate confidently with global stakeholders.
  • Working knowledge of publication management tools and standard document management systems.

PREFERRED QUALIFICATIONS

  • •ISMPP / CMPP certification or publication management credentials
  • •Hands-on experience with abstract, poster and manuscript congress submissions
  • •Familiarity with Veeva Vault and other regulated content platforms
  • •Exposure to vaccines, immunology or specialty care therapeutic areas
  • •Agile or Lean Six Sigma process improvement experience

REQUIRED VERIFIED SKILLS

Medical Communications & Publication Planning
Project Management (timelines, milestones, risk tracking)
iEnvision / Datavision Publication Management
PromoMats & NAYA Compliance Workflows
Scientific & Medical Writing Support
Global Stakeholder Management
Budget & External Spend Tracking
ICH-GCP / GPP3 Publication Compliance
Therapeutic Area Domain Knowledge
MS Project, Excel & SharePoint Reporting

COMPENSATION & REWARDS

Salary: Competitive / Disclosed upon candidate shortlisting

ORGANIZATION CONTEXT & CULTURE

Sanofi is a global biopharmaceutical company dedicated to human health. It researches, develops, manufactures, and markets innovative therapeutic solutions with a focus on specialty care, vaccines, general medicines, and consumer healthcare products. The company aims to prevent and treat a wide range of diseases worldwide.

TEAM SIZE: Approximately 90,000 employees
INDUSTRY: Pharmaceuticals / Biotechnology

EXPECTED CAREER ROADMAP

Within two to three years, a strong performer typically progresses to Project Specialist or Senior Project Specialist, owning larger publication portfolios and eventually stepping into Medical Communications Manager or Publications Lead roles with accountability for budgets, vendors and therapy-area strategy. Sanofi's Hyderabad hub also offers lateral moves into scientific writing, medical affairs operations, HEVA or clinical documentation. Beyond Sanofi, the experience transfers readily to global medical communications agencies, CROs, other pharma capability centres and health-tech content teams, where publication professionals are in steady demand. Professionals who add ISMPP certification and hands-on writing samples often accelerate into fully fledged Medical Writer or Publications Manager positions, with hybrid and remote opportunities increasingly common across India.

APPLICATION ADVISORY

Tailor your CV around delivery metrics — number of publications or medical education assets coordinated, therapy areas covered, tools used (iEnvision, PromoMats, NAYA, Veeva Vault) and budget sizes managed. For interviews, prepare to discuss publication planning timelines, GPP3 and ICH-GCP compliance basics, how you handle reviewer comments under tight deadlines, and how you manage difficult global stakeholders. Expect scenario questions on risk escalation and vendor spend tracking. Bring one or two anonymised examples showing how you improved turnaround time or quality within a medical writing workflow.

READY TO SUBMIT?

Verify your capability profile and matching credentials before submitting direct applications.