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Company Description
IntelliMed is a Singapore based organisation , a trusted partner to 55+ leading Indian pharmaceutical companies and 10+ multinational organizations, with project experience spanning 18+ countries. Supported by a leadership team comprising experienced medical and allied healthcare professionals, we provide comprehensive scientific and medical communication solutions across 18+ therapy areas covering the Pharmaceutical, Nutraceutical, Nutrition, and Medical Device sectors.
Executive/Sr.Executive – Evidence Generation
Experience: Minimum 1-2 years of relevant experience in clinical research
Location: Mumbai (office based)
Qualification : M.Pharm / B.Pharm / M.Sc with clinical research experience or certification in clinical research
As an Executive/Sr.Executive – Evidence Generation, you will be responsible for supporting the design, execution, and dissemination of real-world evidence (RWE) studies and other evidence-generation activities across multiple therapeutic areas. You will collaborate with client POCs (marketing & medical), investigators, internal teams (project management, accounts & finance, medical writer, statistician, data entry), Ethics Committee, external partners (CRO) and clinical research coordinators (CRCs).
Key Responsibilities
Protocol development, CRF, site coordination, data collection, and reporting across multiple therapeutic areas.
Ethics committee submission
Collaborate with client stakeholders (medical and marketing teams) to understand evidence needs and ensure alignment of study objectives with business and scientific goals.
Investigator selection and protocol briefing
Coordinate with internal departments such as the project management, accounts & finance, medical writing, statistics, and data entry to ensure seamless project execution.
Monitor clinical research activities
Liaise with contract research organizations (CROs)
Monitor project timelines and deliverables
Client communications and study updates
Support data review and interpretation in collaboration with statisticians and medical writers for the preparation of scientific publications, abstracts, and presentations.
Internal knowledge-sharing sessions to support strategic decision-making and operational excellence.
Technical Skills
1.Knowledge of Real-World Evidence (RWE) Methodologies – Understanding of observational, retrospective, prospective, and registry-based study designs.
2.Protocol and Document Development – Experience drafting or reviewing protocols, CRFs, ICFs, and EC submission documents.
3.Regulatory and Ethical Understanding – Familiarity with ICH-GCP and EC processes.
4.Stakeholder Coordination – Ability to coordinate with investigators, CRCs, CROs, and internal departments to ensure smooth study execution.
5.Project Management – Managing study timelines, milestones, and budgets using project management tools or trackers.
6.Scientific and Medical Writing Support – Assisting in data interpretation and supporting preparation of manuscripts, abstracts, and reports.
7.Basic Data Handling and Quality Checks – Familiarity with data entry processes, understanding of common data errors, and QC protocols.
8.MS Office Proficiency – Advanced skills in Word, Excel (trackers, pivot tables), PowerPoint (for presentations), and Outlook.
Soft Skills
1.Communication Skills
2.Collaboration & Teamwork
3.Attention to Detail
4.Problem Solving & Critical Thinking
5.Time Management & Multitasking
6.Client-Centric Mindset
7.Adaptability & Learning Agility
8.Professionalism & Ownership
