This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
Seeking a Principal Medical Writer, Patient Safety for a remote role based in Bengaluru, India. You will independently lead complex aggregate safety reports, serving as a subject matter expert on regulatory submissions. Requires strong analytical skills, exceptional medical writing, and client-fo...
Location
India , Remote, Bengaluru
Salary
Not provided
Parexel
Expiration Date
Until further notice
Senior Medical Writer, Patient Safety
Senior Medical Writer, Patient Safety role in Bengaluru, India. Lead the preparation of complex aggregate safety reports (PSURs, PBRERs, DSURs) and drive strategic safety submissions. Requires expertise in pharmacovigilance regulations and signal detection. Join a team focused on global complianc...
Location
India , Bengaluru
Salary
Not provided
Parexel
Expiration Date
Until further notice
Senior Regulatory Affairs Associate
Senior Regulatory Affairs Associate sought for Parexel Consulting to lead radiopharmaceutical lifecycle management. Leverage expertise in CMC authoring, safety labelling, and Health Authority submissions. This remote role based in India offers flexible work, global client exposure, and mentorship...
Location
India
Salary
Not provided
Parexel
Expiration Date
Until further notice
Principal Physician, Patient Safety
Seeking a Principal Physician, Patient Safety in India to lead drug safety expertise. This role requires clinical medicine experience and deep knowledge of drug development and global safety regulations. You will manage adverse event profiles, act as a Subject Matter Expert, and collaborate with ...
Join Parexel Consulting as a **Regulatory Affairs Associate** specializing in **Annual Reports & Renewals for Biologics**. Leverage your 2-4 years of **Regulatory Affairs-CMC** experience to support global submissions (US/EU/Brazil/LATAM/China). Work remotely from India, collaborating with cross-...
Seeking a **Regulatory Affairs Consultant** in Bengaluru, India. Leverage 5+ years of experience in pharmaceutical/biotech compliance to manage third-party partner relationships. Ensure regulatory oversight, develop risk mitigation strategies, and monitor partner performance. Enjoy flexible remot...
Location
India , Bengaluru
Salary
Not provided
Parexel
Expiration Date
Until further notice
Senior Regulatory Affairs Associate
Join Parexel as a Senior Regulatory Affairs Associate. Utilize your expertise in EU procedures, labeling variations, and Veeva to help clients navigate complex regulations. Enjoy remote work in India with a supportive team, global client exposure, and mentorship for career growth.
Location
India
Salary
Not provided
Parexel
Expiration Date
Until further notice
Senior Clinical Database Programmer
Seeking a Senior Clinical Database Programmer for a remote role in India. You will design and maintain high-quality clinical databases using Oracle InForm/Rave EDC, ensuring data integrity. This position requires 5+ years of pharma/CRO experience, Rave Custom Function skills, and offers mentorshi...
Location
India , Remote
Salary
Not provided
Parexel
Expiration Date
Until further notice
Database Administrator
Location
India
Salary
Not provided
Parexel
Expiration Date
Until further notice
Supply and Logistics Coordinator
Location
India , Remote
Salary
Not provided
Parexel
Expiration Date
Until further notice
Senior Integration Engineer
Seeking a Senior Integration Engineer in India with MuleSoft 4 certification and 7+ years' software engineering experience. You will design and develop high-quality APIs and integrations using MuleSoft Anypoint Platform. The role requires expertise in SOAP/REST, EIP patterns, and CI/CD within an ...
Location
India
Salary
Not provided
Parexel
Expiration Date
Until further notice
Quality Manager
Seeking an experienced Quality Manager to support global Biostatistics and Programming teams, with a focus on India. You will lead Quality Event support, audits, SOP updates, and consultancy, requiring 8-12 years in clinical research and expertise in ICH-GCP and CAPA. This role offers a key partn...