Aizant Drug Hiring a Medical Writer

Medical Writer Clinical Pharmacology Jobs Hyderabad

Aizant Drug Research hiring Medical Writer (Clinical Pharmacology) in Hyderabad. B.Pharm, M.Pharm, PharmD with 1–3 years experience.

Aizant Drug Research Solutions Pvt. Ltd. is inviting applications from qualified pharmacy professionals for the role of Medical Writer – Clinical Pharmacology at its Hyderabad facility. This opportunity is ideal for candidates seeking long-term growth in regulatory medical writing, clinical research documentation, and global regulatory submissions within a well-established CRO environment.

This role is particularly relevant for candidates actively searching for medical writer jobs in Hyderabad, clinical pharmacology jobs, regulatory medical writing roles, and pharma clinical research careers. The position offers exposure to global regulatory standards, multidisciplinary collaboration, and career advancement in clinical documentation and regulatory affairs.

Company Overview

Aizant Drug Research Solutions Pvt. Ltd. is a leading integrated pharmaceutical and clinical research organization providing end-to-end services across formulation development, analytical research, clinical research, regulatory affairs, and medical writing. The organization is known for its strong compliance culture, adherence to global regulatory guidelines, and consistent delivery of high-quality scientific and regulatory documentation.

With a robust presence in clinical pharmacology, bioequivalence, and regulatory sciences, Aizant supports pharmaceutical, biotechnology, and healthcare companies across domestic and international markets. The company emphasizes scientific accuracy, regulatory compliance, and professional development, making it a preferred employer for life sciences professionals.

Job Role & Responsibilities

As a Medical Writer – Clinical Pharmacology, the selected candidate will be responsible for preparing, reviewing, and managing clinical and regulatory documents in accordance with international regulatory standards. The role demands strong scientific writing skills, regulatory knowledge, and attention to detail.

Key responsibilities include:

• Drafting, editing, and reviewing clinical study protocols, investigator brochures, informed consent forms, and clinical study reports
• Preparing regulatory submission documents including INDs, NDAs, CTDs, briefing documents, and related modules
• Ensuring accuracy, clarity, and consistency across all clinical and regulatory documentation
• Maintaining compliance with ICH-GCP guidelines, regulatory requirements, and internal SOPs
• Collaborating with cross-functional teams such as clinical research, biostatistics, regulatory affairs, and medical affairs
• Participating in project meetings, contributing to timelines, and supporting deliverables
• Maintaining document version control and adherence to approved templates and style guides

Eligibility / Qualifications

Educational qualifications required for this role include:

B.Pharm, M.Pharm, PharmD

Candidates must possess:

• Strong knowledge of clinical research processes and regulatory requirements
• Excellent written and verbal communication skills in English
• Proficiency in Microsoft Office and document management systems
• Ability to interpret scientific data and translate it into clear regulatory documentation

Desired Skills & Competencies

• Hands-on experience with regulatory submissions to agencies such as FDA, EMA, or other global authorities
• Familiarity with medical terminology, clinical pharmacology concepts, and basic statistical principles
• Ability to adapt writing style for scientific, regulatory, and patient-facing audiences
• High attention to detail and commitment to document accuracy and data integrity
• Strong organizational skills and ability to manage multiple documents simultaneously

Location & Work Environment

Job Location: Dulapally, Hyderabad

The role is based at Aizant’s Hyderabad facility, offering a professional work environment with exposure to global clinical research projects and regulatory documentation workflows.

Application Process

Interested and eligible candidates are invited to apply by sharing their updated CV via email.

Email: sonyeevitha.degala@aizant.com

Applicants are advised to mention the position title “Medical Writer – Clinical Pharmacology” in the subject line for faster shortlisting.

Frequently Asked Questions (FAQs)

Who can apply for this Medical Writer role?
Candidates with B.Pharm, M.Pharm, or PharmD qualifications and 1–3 years of relevant experience in medical or regulatory writing can apply.

Is prior regulatory submission experience mandatory?
Prior experience with FDA, EMA, or global regulatory submissions is preferred but not mandatory.

Is this role suitable for freshers?
This position is intended for candidates with some professional experience. Fresh graduates may not be considered.

What is the career growth path in medical writing at Aizant?
Aizant offers structured growth into senior medical writer, regulatory specialist, and leadership roles based on performance and experience.

Company                     Aizant Drug Research Solutions Pvt. Ltd.
Vacancies                     Not Disclosed
Required Education     B.Pharm, M.Pharm, PharmD
Experience                   1–3 Years