Parexel
Company Overview
Parexel is a global biopharmaceutical services organization supporting pharmaceutical and life sciences companies across clinical development, regulatory and commercialization-related activities.
This Medical Writer I – Patient Safety opportunity is aligned with the company's patient-safety and pharmacovigilance activities.
The position offers exposure to multiple areas of safety medical writing, including:
Aggregate safety reporting
Signal detection and signal management
Risk Management Plans
Safety literature review
Regulatory safety documentation
Safety-data analysis
Global pharmacovigilance requirements
Quality control
Regulatory submissions
Inspection readiness
The role can be particularly relevant for candidates who want to build a career in Pharmacovigilance Medical Writing, Drug Safety, Aggregate Reporting and Patient Safety.
Work Culture & Hiring Values
At Parexel, employee growth is prioritized alongside business targets. Teams follow an agile development lifecycle with horizontal leadership patterns, encouraging open questions and product innovation. Active learning pathways, project mentorship programs, and structured career reviews ensure you continue to gain highly marketable skills.
Active Job Openings (6)
Medical Writer
Parexel's Medical Writing team supports the development of important clinical and regulatory documents used throughout the drug development lifecycle. For Medical Writer I, the focus is on developing, editing, and reviewing clinical documentation, supporting literature research, analyzing study information, and working with cross-functional teams.
Senior Medical Writer
Parexel's Medical Writing team supports the development of important clinical and regulatory documents used throughout the drug development lifecycle. For Senior Medical Writer, the role involves taking greater ownership of complex regulatory documents, interpreting clinical and statistical information, coordinating review processes, managing timelines, and supporting junior writers. Both opportunities require strong scientific communication skills, attention to detail, and the ability to work effectively with multidisciplinary teams.
Senior Regulatory Affairs Associate
A Senior Associate must have an understanding of the organization's basic consulting models and methodologies, as well as basic knowledge of what services PC provides. A Senior Associate must be technically competent and continually developing the skills as defined in the key accountabilities section of this document. A Senior Associate, under the general direction of a Project Lead and/or Technical SME, takes responsibility for ensuring that client work is performed, and delivered on time, mee...
Clinical Research Associate II/ Senior - FSP
FSP CRA Opportunity with at least 3 years of CRA experience from Australia/ New Zealand Location to be based: NSW or VIC Key Accountabilities : Oversight of Monitoring Responsibilities and Study Conduct Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and client standards to achieve project goals, timelines and quality Manage assigned operational aspects for implementation of clinical trial activities at assigned ...
Regulatory Affairs Consultant
A Consultant must have an understanding of the organization's consulting models and methodologies, as well as, good knowledge of what services PC provides. A consultant must have strong technical skills and may be developing specialist knowledge of a particular subject and/ or market. A Consultant ensures the timely performance of work within a project scope to the quality expectations of PC and the client. When serving as a Project Lead or Work Stream Lead, a Consultant assures the work of the...
Medical Writer I – Patient SafetyCompany Name: Parexel
Parexel is hiring for a Medical Writer I – Patient Safety position in India, with opportunities listed for Hyderabad, Bengaluru and Bengaluru-Remote. The role is focused on preparing and supporting scientific and regulatory safety documentation within the pharmacovigilance function. The selected professional may work on aggregate safety reports, signal management, risk management documentation, literature reviews and safety-data analysis. Candidates with backgrounds in Pharmacy, Life Sciences, Biomedical Sciences and related healthcare disciplines are eligible to be considered. Prior pharmacovigilance experience is preferred, while the supplied job information does not specify a fixed minimum number of years.
Company Directory
The supplied vacancy mentions work locations in:
Hyderabad, India
Bengaluru, India
Bengaluru-Remote, India
A specific office street address was not provided in the supplied job information.