Roles & Responsibilities

Key Responsibilities:

Drive client acquisition and growth by identifying prospects, qualifying leads, supporting pitches, and contributing to proposals, SOWs, budgets, and timelines.

Build and maintain strong client relationships to enable repeat business, project expansion, and effective understanding of scientific and commercial needs.

Collaborate with leadership on pricing strategy, service positioning, and market intelligence while representing the organization at scientific and industry events.

Lead end-to-end planning and execution of scientific and medical projects across medical writing, RWE studies, and advisory/consensus initiatives.

Coordinate cross-functional teams and served as the primary client point of contact to ensure on-time, within-scope, and compliant project delivery.

Oversee project governance, including timelines, risk management, KPI tracking, quality control, documentation, and audit-ready records.

Requirements:

Bachelor s degree in Medicine or Pharmacy, Master's degree or a PhD is a plus.

3 6 years of experience in medical communications, clinical research, CROs, pharmaceutical companies, or scientific consultancy.

Proven experience in scientific project coordination or management within healthcare or life sciences, including client management and proposal/SOW development.

Strong scientific background with solid understanding of clinical research, medical writing, evidence generation, and publication processes.

Familiarity with real-world evidence (RWE), observational studies, and advisory or consensus projects.

Strong communication, stakeholder management, and client-facing leadership skills with commercial awareness.

Excellent organizational and multitasking skills.

High attention to detail with a strong focus on quality.

Ability to work independently and collaboratively in a fast-paced environment.

Excellent written and verbal communication skills in English.

Desired Candidate Profile

Bachelor s degree in Medicine or Pharmacy, Master's degree or a PhD is a plus.

3 6 years of experience in medical communications, clinical research, CROs, pharmaceutical companies, or scientific consultancy.

Proven experience in scientific project coordination or management within healthcare or life sciences, including client management and proposal/SOW development.

Strong scientific background with solid understanding of clinical research, medical writing, evidence generation, and publication processes.

Familiarity with real-world evidence (RWE), observational studies, and advisory or consensus projects.

Strong communication, stakeholder management, and client-facing leadership skills with commercial awareness.

Excellent organizational and multitasking skills.

High attention to detail with a strong focus on quality.

Ability to work independently and collaboratively in a fast-paced environment.

Excellent written and verbal communication skills in English.

Company Industry

Consulting / Management Consulting / Advisory Services

Department / Functional Area

Doctor / Nurse / Paramedics / Hospital Technicians / Medical Research