Are you passionate about advancing healthcare through scientific writing? If so, Parexel, a global leader in clinical research and development, is offering an excellent opportunity for talented professionals to join their team as a Medical Writer II. This full-time position is available across multiple locations in India, including Mohali, Bengaluru, Hyderabad, and remote options, making it an ideal choice for those seeking rewarding Pharma Jobs in 2025. Posted on February 20, 2025, this job opening aligns with Parexel’s mission to improve global health through innovative clinical solutions.
At Pharmabharat.com, we are committed to bringing you the latest Pharma Job Opportunities in India and beyond. Read on to explore this exciting role, its responsibilities, qualifications, and how you can apply to kickstart your career with Parexel.
Why Choose Parexel for Pharma Jobs?
Parexel is a renowned name in the pharmaceutical and clinical research industry, offering cutting-edge solutions in clinical trials, regulatory consulting, and market access. Joining Parexel as a Medical Writer II means contributing directly to therapies that benefit patients worldwide. With a strong emphasis on empathy and quality, this role is perfect for professionals who thrive in a purpose-driven environment.
This position offers flexibility with locations in India-Mohali, India-Bengaluru, India-Hyderabad, and remote options, catering to diverse lifestyles. Whether you’re based in a bustling city or prefer working from home, Parexel ensures you can excel in your career while maintaining work-life balance.
Key Responsibilities of a Medical Writer II
The Medical Writer II role at Parexel is dynamic and multifaceted, focusing on the preparation and management of critical safety and regulatory documents. Here’s a snapshot of what the job entails:
- Aggregate Reports: You’ll manage scheduled and unscheduled reports such as Periodic Safety Update Reports (PSURs), Periodic Benefit-Risk Evaluation Reports (PBRERs), Development Safety Update Reports (DSURs), and more. This includes drafting, updating Risk Management Plans (RMPs), and ensuring compliance with global regulatory standards.
- Clinical Study Report (CSR) Narratives: You’ll write clear, accurate narratives based on clinical and safety data, collaborating with study teams to ensure medical cohesiveness and quality.
- Signal Detection and Management: Perform qualitative and quantitative signal detection from various sources, including regulatory databases and literature, while leading signal assessment processes.
- Compliance and Coordination: From generating line listings to conducting quality reviews and coordinating meetings, you’ll ensure high-quality deliverables and timely submissions to health authorities.
This role demands excellent organizational skills, attention to detail, and the ability to work collaboratively in a team-oriented environment—qualities that make it a standout among Medical Writer Jobs.
Skills and Qualifications Required
Parexel is seeking candidates with a strong background in life sciences or healthcare. Here’s what you need to qualify for this Pharma Job:
- Education: A university degree in Life Sciences, Pharmacy, Biotechnology, Biochemistry, or a related field is required. A medical background (e.g., Medicine, Nursing, Dentistry) with patient exposure is an advantage.
- Experience: Prior experience in regulatory writing, pharmacovigilance, or a related field is desirable. Familiarity with medical terminologies and global drug safety regulations is a must.
- Skills: Analytical thinking, excellent communication (written and verbal), and proficiency in Microsoft Office and web-based applications are essential. Fluency in English and the ability to manage multiple tasks efficiently are also key.
Parexel values a client-focused approach, problem-solving abilities, and a flexible attitude—attributes that will help you shine in this role.
