Sr Medical Writer (Redaction)

Syneos Health; Madurai; On-site; INR 1,200,000 - 1,800,000; Full time

Benefits offered by this job

Career Development

Training and Recognition

Diversity and Inclusion Programs

Job summary

A leading biopharmaceutical solutions organization is seeking a Sr Medical Writer to join their Clinical Trial Disclosure team. This role involves authoring and ensuring quality of complex clinical documents, while also mentoring junior team members. The ideal candidate will have a strong background in medical writing and a scientific degree, along with excellent analytical and communication skills.

Qualifications

• 4-8 years of experience as a medical writer.
• Familiar with clinical document redaction and anonymization.

Responsibilities

• Authoring clinical study reports and regulatory submissions.
• Performing quality control and document reviews.
• Training and mentoring team members.

Skills

Analytical

Communication

Team Collaboration

Education

Scientific Graduate Degree

Job description

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Job Overview

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We focus on translating clinical, medical affairs, and commercial insights into outcomes that address modern market realities.

Our Clinical Development model centers on the customer and patient, aiming to simplify and streamline processes to enhance our services and work environment. Whether in a Functional Service Provider partnership or a Full-Service setting, our team collaborates passionately to help our clients achieve their goals. We are agile and committed to accelerating therapy delivery to improve lives.

Why Work at Syneos Health

• We invest in our people’s career development, training, recognition, and rewards.
• Our Total Self culture encourages authenticity and inclusivity.
• We foster diversity and create a sense of belonging across our global team.

Job Summary

The Clinical Trial Disclosure team plays a vital role in executing projects involving complex scientific, medical, and technical information processing for our global clients.

Key Responsibilities

• Authoring and quality assurance of project documents, including clinical study reports, patient narratives, and summaries for regulatory submissions (EMA, Health Canada, EUCTR, NIH).
• Performing QC and reviews of documents against checklists and SOPs.
• Analyzing processes and outputs, ensuring compliance with client procedures.
• Training and mentoring team members as needed.

Qualifications

• 4-8 years of experience as a medical writer involved in clinical document redaction and anonymization, familiar with relevant regulations.
• Experience with clinical trial disclosure documents, including registration forms for clinicaltrials.gov.
• Educational background in life sciences (minimum scientific graduate degree).
• Knowledge of regulatory requirements, clinical development, ICH-GCP, and basic computer skills.
• Strong analytical, communication, and team collaboration skills.

Additional Information

Role may include other duties as assigned. We value equivalent experience and are committed to compliance and diversity. The position is full-time, mid-senior level, within the biotech and pharma industries.