Senior Associate – Scientific Writing
Location: Karnataka, India
Date Posted: 12 November 2025
Hiring Company: Technology-Led Global Healthcare Solutions Provider
Experience Required: Fresher (0 years). Candidates with academic research, internships, scientific writing exposure, or healthcare domain familiarity will be considered an advantage.
About the Role
We are a global, technology-driven healthcare solutions organization focused on helping healthcare companies become future-ready. Our teams work at the intersection of healthcare, science, and digital innovation. This role offers an opportunity to begin a fast-track career, gain exposure to global medical writing standards, and be mentored by experienced professionals.
The Senior Associate – Scientific Writing will support the development, review, and coordination of clinical and regulatory documents. This position is ideal for freshers looking to start a career in scientific writing within a high-growth, knowledge-driven environment.
Educational Qualification
Candidates must hold a degree in one of the following:
MBBS, PhD, MDS, BDS, MPharm, PharmD
Key Responsibilities
• Assist in preparing and reviewing clinical study reports, protocols, investigator brochures, and submission-related data summaries
• Apply structured and lean authoring principles to develop high-quality regulatory documents
• Support document review activities, quality checks, and version finalization
• Contribute to project plans and maintain document timelines
• Participate in cross-functional team discussions and document kick-off meetings
• Ensure adherence to standard templates, best practices, and regulatory expectations
• Assist in addressing feedback received during document review cycles
• Conduct literature searches and scientific data screening as required
• Support departmental initiatives and continuous improvement activities
• Maintain compliance with organizational training and documentation policies
Required Skills
• Understanding of clinical development basics, study design, and regulatory documentation
• Ability to work with templates, style guides, and structured processes
• Strong written communication and scientific comprehension
• Good organizational, time-management, and interpersonal skills
• Ability to collaborate effectively with internal teams and stakeholders
• Willingness to learn new tools, technologies, and authoring systems
Scientific Knowledge Expectations
• Awareness of global regulatory frameworks, including guidelines from the US and EU
• Ability to interpret clinical data and apply scientific logic for document drafting
• Understanding of therapeutic areas, drug development concepts, and medical terminology
• Capability to ensure content consistency and alignment with project strategy
• Ability to support argument development in scientific and regulatory contexts
Technology Skills (Good to Have)
• Proficiency in MS Word and familiarity with document formatting standards
• Experience using document management systems and workflow tools (optional for freshers)
• Understanding of Word add-ins used for style, reference, or template management
• Openness to learning new digital tools used in medical writing environments
Why Join Us
• Global exposure to regulatory writing and medical documentation
• Structured learning, mentorship, and rapid career progression for fresh talent
• Opportunities to work with cross-functional teams across scientific and digital domains
• A purpose-driven environment that emphasizes innovation, collaboration, and professional growth
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