samahitha Hiring Medical Writer

Life Sciences — Medical Writer (1+ yrs) — Immediate Joiner

Life science grads: Medical Writer role (1+ yrs experience). Immediate joining. Send CV to career@samahitha.com.

Samahitha Research Solutions is hiring a Medical Writer with 1+ years of hands-on experience and immediate availability. This role is ideal for life-science graduates who can translate clinical and scientific data into clear, regulatory-compliant documents. As a Medical Writer at Samahitha, you will support clinical teams and senior writers in preparing study reports, protocols, and regulatory submissions that underpin safe and effective patient care.

Company Overview

Samahitha Research Solutions provides clinical research support and scientific communications services to sponsors, CROs, and investigator sites. The company focuses on quality-driven documentation, adherence to regulatory standards, and timely delivery of scientific outputs. Joining Samahitha means working in a collaborative environment where medical writing contributes directly to trial integrity, regulatory acceptance, and evidence dissemination.

Job Role & Responsibilities

Position: Medical Writer (Officer / Associate level)

As a Medical Writer, you will support preparation and maintenance of clinical and regulatory documents under supervision. Typical deliverables and tasks include:

• Draft and format clinical study reports (CSRs), protocols, investigator brochures (IBs), informed consent forms (ICFs), and other regulatory documents following templates and company style guides.
• Conduct structured literature searches and evidence reviews; summarize and synthesize scientific findings relevant to assigned therapeutic areas.
• Prepare concise summaries for clinical and safety data, including tables, figures, and legends compatible with regulatory submission formats.
• Support senior writers with statistical appendices, methodology descriptions, and interpretation of clinical results for inclusion in CSRs and regulatory dossiers.
• Maintain accurate version control, track reviewer comments, and implement feedback from cross-functional teams including clinical operations, data management, biostatistics, and regulatory affairs.
• Assist with preparation of presentations, slide decks, abstracts, and posters for conferences and internal communications.
• Ensure all documents comply with ICH and GCP guidelines, local regulatory expectations, and company SOPs for medical writing and data integrity (ALCOA+ principles).
• Help maintain document templates, a reference library, and style guide consistency across projects.
• Participate in review meetings and contribute to timelines and project trackers to ensure on-time delivery.

This role blends scientific rigor with clear written communication and requires a methodical approach to manage multiple documents and deadlines.

Eligibility / Qualifications

• Education: Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, Microbiology, Medicine, or a related field.
• Experience: Minimum 1 year in medical writing, scientific writing, regulatory documentation, or a related role supporting clinical trials or publications.
• Technical skills: Familiarity with clinical trial documents (protocols, CSRs, ICFs), basic understanding of clinical trial design and biostatistics, and proficiency in MS Word, PowerPoint, and reference managers (EndNote, Mendeley). Exposure to eCTD or regulatory submission workflows is a plus.
• Soft skills: Excellent written English, attention to detail, capacity to interpret clinical data, good interpersonal skills for cross-functional collaboration, and ability to work under tight deadlines.

Relevant courses (comma-separated): B.Sc Life Sciences, M.Sc Life Sciences, B.Pharm, M.Pharm, B.Sc Biotechnology, M.Sc Biotechnology, MBBS, PG Diploma in Clinical Research, Certificate in Medical Writing, MSc Clinical Research

Location & Salary

• Location: Bangalore (office-based / hybrid options subject to company policy).
• Salary: Not specified in the HR brief. Compensation will be competitive and commensurate with experience and skill level.

Application Process

Interested candidates should email their CV to:

• Email: career@samahitha.com

Email subject suggestion: Application — Medical Writer — [Your Name]

In your application, highlight: therapeutic areas you’ve worked in, examples of documents you contributed to (e.g., CSR sections, protocols), and your notice period/availability for immediate joining.

How to Prepare a Strong Application

• Provide a tailored CV focused on medical writing experience: list specific document types and your role in each (drafting, editing, formatting).
• Include (or be ready to provide) writing samples or redacted excerpts showing scientific clarity and formatting skills. If samples cannot be shared, summarize the documents and your contributions.
• Highlight any experience with literature reviews, reference management, tables/figures generation, and interaction with biostatistics and clinical teams.
• Make availability clear — this role prioritizes immediate joiners.

Why this role matters (EEAT Alignment)

Medical writing is the backbone of clinical communication. Clear, accurate, and well-structured documents enable regulatory reviewers to assess safety and efficacy evidence. This role directly impacts product approvals, ethical trial conduct, and transparent dissemination of clinical findings. By ensuring documents meet regulatory standards and scientific rigor, medical writers build organizational expertise and credibility — essential elements of Google’s E‑A‑T framework.

High-Value Keywords Included Naturally

medical writer jobs, clinical study report writer, regulatory medical writing, medical writing jobs Bangalore, protocol writing, CSR writing careers, scientific writing in pharma, ICH GCP medical writing.

FAQs

Q: Is 1 year of experience sufficient?
A: Yes. This role requires a minimum of 1 year in medical/scientific writing or supporting clinical documentation.

Q: Are writing samples required?
A: If available, include redacted samples. If not, describe your contributions to documents in the CV and be ready to provide examples upon request.

Q: Will there be training?
A: Expect on-the-job training and mentorship from senior medical writers, especially on company templates and regulatory expectations.

Q: What software skills are important?
A: Strong MS Word and PowerPoint skills are essential. Familiarity with reference managers (EndNote, Mendeley) and basic table/figure preparation is beneficial.

Q: Is the role remote or on-site?
A: Location listed is Bangalore. Work model (on-site/hybrid) depends on company policy and will be clarified during hiring.

Closing Note

If you can translate complex clinical data into accurate, regulation-ready documents and are available to join immediately, Samahitha’s Medical Writer position offers a practical, high-impact role to build your career in clinical communications and regulatory support.

---

Category	Details
Company	Samahitha Research Solutions
Vacancies	Medical Writer — Immediate Joiner
Required Education	Life Sciences, Pharmacy, Biotechnology, Microbiology, MBBS, Clinical Research courses
Experience	1+ year