Job Title: Senior Scientific Writer
Job ID: REQ-10068651
Job Category: Medical Writing | Scientific Communications | Clinical Research & Development
Location: Hyderabad, Telangana, India (Hybrid)
Employment Type: Full-Time | Regular
Industry: Pharmaceutical | Life Sciences | Clinical Research
Experience Required: 4–10+ Years (depending on qualification)
ThePharmaDaily.com presents a senior-level opportunity for an experienced Senior Scientific Writer to join a global pharmaceutical leader in Research & Development. This role is critical in delivering high-quality scientific publications and medical content, supporting clinical research, regulatory communication, and global medical strategies.
The position involves end-to-end ownership of scientific content, from initial briefing through final publication or presentation, ensuring first-time-right delivery aligned with the Scientific Communication Plan (SCP).
Develop high-quality scientific content, including:
Abstracts, manuscripts, posters, and presentation slide decks
Subgroup analyses and RWE/observational study publications
Medical education materials and foundational scientific content
Congress-related deliverables (pre-congress materials, onsite coverage, post-congress decks, omni-channel content)
Conduct literature searches, publication alerts, and congress communications
Support medical education and scientific storytelling aligned with defined scientific narratives
Perform quality control (QC) and proofreading to meet internal and external standards
Ensure compliance with regulatory, publication, and journal standards (e.g., CONSORT guidelines)
Follow company specifications, templates, SOPs, and documentation standards
Maintain audit readiness, training compliance, and accurate project archiving
Manage multiple projects across up to two brands simultaneously
Obtain and incorporate feedback from internal and external stakeholders
Adhere to project management tools, policies, and timelines
Build and maintain strong working relationships with clinical, regulatory, and medical teams
Candidates must meet one of the following qualification and experience combinations:
B.Sc. or equivalent with 8+ years of Clinical Research experience
M.Sc. / M.Pharm with 6+ years of Clinical Research experience
PhD with 4+ years of Clinical Research experience
MBBS or equivalent with 4+ years of Clinical Research experience
MD or equivalent with 2+ years of Clinical Research experience
Strong expertise in medical and scientific writing for clinical research publications
Proven ability to deliver regulatory and journal-ready documents within timelines
Excellent written and verbal communication across diverse audiences
High attention to detail with strong quality and compliance orientation
Ability to manage multiple priorities in a fast-paced, global environment
Strong collaboration and stakeholder management skills
Experience in process optimization and continuous improvement
Ability to build trusted relationships with internal and external partners
Strong understanding of global publication strategies and medical compliance
Work on global, high-impact clinical and scientific publications
Be part of a leading pharmaceutical R&D organization
Hybrid work environment with strong focus on quality, innovation, and collaboration
Career growth in medical writing, scientific communications, and clinical development
Inclusive culture committed to diversity, equity, and patient-centric innovation
The organization is committed to building an inclusive workplace and diverse teams that reflect the patients and communities it serves. Equal opportunities are provided to all qualified candidates.
Gujarat :
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