Medical Editor Ii Clin Pharm (Editing Of Csr, Ib, Protocol)

Syneos Health

2-4 years

Not Disclosed

India Remote

10 Jan. 5, 2026

Job Description

Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Medical Editor II – Clinical Pharmacology (CSR, IB, Protocol Editing) | Remote – India

Location: Remote, India
Job Type: Full-Time
Job ID: 25104357

About Syneos Health

Syneos Health® is a global, fully integrated biopharmaceutical solutions organization, delivering clinical development and commercial services that accelerate drug development and improve patient outcomes. With 29,000 employees across 110 countries, we collaborate with sponsors, investigators, and cross-functional teams to streamline clinical and medical writing processes while ensuring regulatory compliance.

We foster a culture of career growth, mentorship, and diversity, offering employees training programs, peer recognition, and total rewards to support their professional development.

Role Overview

Syneos Health is seeking an experienced Medical Editor II – Clinical Pharmacology to provide high-quality editing, review, and compilation of clinical study documents. This includes Clinical Study Reports (CSR), Investigator’s Brochures (IB), and Protocols, ensuring accuracy, clarity, and regulatory compliance.

The role is ideal for candidates with strong medical writing or editing experience in clinical pharmacology, excellent command of English, and familiarity with regulatory guidelines such as FDA, EMA, and ICH.

Key Responsibilities

Document Editing & Quality Assurance

Copyedit clinical documents (CSR, IB, Protocols) for grammar, punctuation, spelling, style, and scientific accuracy, following AMA Manual of Style or client-specific guidelines.
Perform quality review of assigned deliverables to ensure content integrity and compliance with sponsor and regulatory requirements.
Ensure consistency across all documents and maintain high editorial standards.

Project & Process Management

Manage assigned projects on time and within budget, adhering to standard operating procedures (SOPs) and client-specific requirements.
Monitor timelines and budgets, updating lead medical writer or project manager if deliverables are at risk.
Compile and assemble medical writing deliverables as required.

Collaboration & Communication

Represent the editorial team in study teams and cross-departmental projects as needed.
Provide feedback to lead medical writers on the progress and quality of editorial work.
Foster constructive collaboration with medical writing leadership and project teams.

Required Qualifications & Experience

Education:

Bachelor’s degree in life sciences, pharmacy, or related field. Advanced degree preferred.

Experience:

Minimum 2–4 years of experience in medical editing or scientific writing, ideally within clinical pharmacology or clinical development.
Experience editing CSR, IB, Protocols, and other regulatory documents is preferred.

Skills & Competencies:

Excellent written and verbal communication skills in English.
Strong knowledge of regulatory guidelines (FDA, EMA, ICH) and medical writing best practices.
Ability to work independently, manage multiple tasks, and meet deadlines.
Attention to detail with a focus on scientific accuracy and editorial quality.

Why Join Syneos Health

Contribute to high-impact clinical and regulatory documents supporting global drug development.
Collaborate with cross-functional teams in a remote and dynamic environment.
Access career development programs, mentorship, and professional growth opportunities.
Work in a culture that values diversity, inclusion, and innovation.

About Syneos Health

Over the past 5 years, Syneos Health has supported 94% of all novel FDA-approved drugs, 95% of EMA-authorized products, and managed 200+ clinical studies across 73,000 sites involving over 675,000 trial patients.

We empower employees to innovate, challenge the status quo, and contribute to life-changing therapies in a competitive global environment.

Apply Now

Advance your career as a Medical Editor II – Clinical Pharmacology (CSR, IB, Protocols) and join a global leader in medical writing and clinical document quality assurance.

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Medical Editor Ii Clin Pharm (Editing Of Csr, Ib, Protocol)

Job Description

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