Project Management Associate
Famor Clinical Research Solutions LLP
This job at a glance
- Who can apply
- Freshers and up to 1 year
- Must know
- Patient careProject managementStakeholder managementBusiness analysis
- Work
- On-site in Hyderabad
- Pay
- Not stated by the employer.
- Skill demand
- Project management73%Stakeholder management60%Business analysis10%Patient care2%of 99 similar fresher jobs posted in India this week
- Listed
- 13 Nov 2026 · still open
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About the Role
Famor Clinical Research Solutions LLP (Famorcr) is a specialized medical writing partner for pharmaceutical, biotech, and clinical research organizations.
This is a remote Project Management Associate internship role that supports the planning, coordination, and tracking of medical writing and clinical documentation projects. The role offers structured mentorship and exposure to project management practices within clinical research and medical writing.
Key Responsibilities
- Assist in defining project timelines.
- Maintain project plans.
- Monitor progress against milestones.
- Coordinate communication among writers, reviewers, and client stakeholders.
- Prepare status reports.
- Document project risks and dependencies.
- Organize project documentation.
- Support process improvement initiatives.
- Contribute to ensuring projects adhere to internal quality and compliance standards.
Requirements & Tech Stack
- Comfort working in distributed teams.
- Proficiency in common productivity and collaboration tools (e.g., project management platforms, document-sharing systems).
Qualifications
- Strong Project Management and Program Management skills, with the ability to support planning, execution, and monitoring of multiple projects.
- Effective Communication abilities, including clear written and verbal communication, stakeholder coordination, and timely status reporting.
- Solid Analytical Skills to interpret project data, identify trends or risks, and support decision-making and process improvements.
- Robust Organization Skills, including attention to detail, documentation management, and time management in a remote environment.
- Interest in clinical research, medical writing, or regulatory affairs; prior exposure through coursework or projects is beneficial.
- Pursuing or holding a degree in life sciences, pharmacy, public health, management, or a related discipline is preferred.