Medical Writer

Company Overview

Syneos Health is a global life sciences services organisation. It works across a spectrum of drug development and industry. Syneos is your next door biopharmaceutical solutions partner. It contributes to customer success using clinical, medical affairs, and commercial insights. This in turn helps therapies reach patients faster.

What makes Syneos relevant for this opening is the kind of operational work it supports. Its Clinical Development services include trial master file support, regulatory and administrative services, safety/pharmacovigilance, and study-startup functions, which means document quality is not a side task here; it is part of the company’s core delivery engine. For candidates looking at non-clinical medical writer jobs in India, that creates a strong entry point into regulated healthcare work without patient-facing responsibilities.

Syneos features an inclusive workplace. It helps employees grow internally instead of simply filling a seat.

A medical writer supports medical documentation, compliance, and project. That makes it useful for life sciences graduates who want a corporate healthcare path with structure, skill-building, and room to move into stronger documentation, clinical operations, or regulatory roles later on.

Job Summary

You will be the main POC for document filing. These may range from compliances, miscellaneous projects and what's inside Veeva RIM and eTMF workflows. Many clinical and research projects generate a large volume of regulated records. You need to fill them correctly, so that other teams can retrieve them when in need.

You will also work on controlled documents, metadata, naming conventions, and filing rules. That makes this an ideal career option for professionals who want non-clinical medical writer jobs in India but still want to stay close to healthcare, regulatory discipline, and scientific operations.

This is also a role where precision has real business value. A clean filing structure must be ready for inspection. This will ensure more seamless handovers and zero delay in meeting deadlines. If you are careful, organised, and comfortable with the workflow, you will find the rhythm of the work very manageable.

This is open for remote position and it is a Gurugram-based organisation. You ought to devote yourself with a full-time schedule and a one-year contract structure.

Key Responsibilities

• Manage regulated document filing inside Veeva RIM.
  
  You ought to place project records into the right location within the system. Keep the setup aligned with client rules. It will further avoid filing gaps. It will keep records usable when audits or reviews come up.

• Support eTMF work with an eye on GxP discipline.
  
  You need to maintain electronic based records like master files. Make sure it goes with the way filing is done. There must be a medical context. You must adhere to regulatory norms.

• Move documents between internal systems and Veeva carefully.
  
  You will download records. Then you will upload them into the correct workspace. You then need to confirm the file is classified properly.

• Check document quality before final filing.
  
  You will review records based on whether they are complete or not. Vet it based on integrity and fundamentals before you can archive it finally. That extra check prevents avoidable rework and protects the quality of the project file.

• Keep project records traceable and up to date.
  
  You will make sure document status is visible. It is important for the documents to be in actual state as it was earlier. This will further help in internal teams to find what they need without getting late.

• Apply naming and metadata rules consistently.
  
  You will validate titles, tags, and filing details so each document lands in the right place the first time. That small habit has a big impact on searchability and archive integrity.

• Work across multiple filing scopes.
  
  You need a fine-tune knowledge of early access programmes. There might be external research projects that you need to be aware of. Some observation based studies are there too.

• Manage your time efficiently.
  
  It is important to manage your time while doing tasks. If there is any issue, please update the Lead Medical Writer or Project Manager. Keep everyone informed and aligned to avoid any issues at the last minute.

• Organise your work and better its flow when you need it.
  
  Get the hang of working with different SOPs. You need to know how to file information in an easy-to-read manner. Handle different types of documents in an organised manner. Be proactive. 

Qualifications and Skills

Must-Have Qualifications

• A Bachelor's degree in Biotechnology or Microbiology or Chemistry or any Life Sciences subjects

• Prior knowledge of regulatory affairs

• You should have the fundamentals of research based learnings

• You must be able to perform in stringent deadlines

Bonus Skills (preferred)

• Knowledge about apps like Veeva or eTMF systems

• Knowledge about medical writing, clinical, or regulatory affairs

Soft Skills & Personality Traits

• Strong attention to detail

• Calm, methodical working style

• Clear communication with project teams

• Ability to learn structured systems quickly

• Reliability when timelines are tight

Salary, Bonuses, & Compensation

Syneos Health is offering around ₹5.0 lakh to ₹6.0 lakh salary per year depending on experience and role scope.

You may get health insurance, paid leave, learning support, and contract-based access to Syneos’ broader development and rewards ecosystem. Syneos’ careers pages specifically emphasize learning and development, inclusive culture, and total rewards.

Location

This opening is listed as Remote (Pre-Approved) and also appears in IND-Gurugram-Hybrid searches. It is a full-time role with a one-year contract structure.

Growth Opportunities

This role can lead into eTMF specialist work, clinical documentation support, project coordination, or wider regulatory operations over time. That path is especially useful for candidates building a long-term career in non-clinical medical writer jobs in India.

Team Structure & Reporting Lines

You will likely work with a Lead Medical Writer, Project Manager, or direct supervisor while coordinating with client stakeholders when needed. The job description also points to regular timeline updates and comment resolution as part of the workflow.

Why This Role Stands Out

This is not just any other medical writing job. It gives you exposure to the industry workflow from the forefront. In any medical writing job, what matters is accuracy. Many internal and external teams will depend on your information to make major decisions.

How to Apply

Are you looking for a job that rewards your expertise in writing medical content? Do you think reading compliances and norms is your daily habit? Then, this job is the best suitable one for you

The best applications for this role must handle documents carefull. He/She/They must know the fundamentals of apps like, Veeva. Practical knowledge of clinical operations is important. A knack for writing on medical sciences is a basic but a rewarding quality for this role.

Before you submit, optimise your CV so it shows the kind of work this role actually needs. Ensure that you are disciplined, detail-oriented comfortable to work in tight deadlines. A focused application will read far better than a crowded one.