Parexel - India, Bengaluru

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...

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...

Associate Manager, Clinical Operations in Bengaluru, India. Oversee clinical trial teams, ensuring high-quality, on-time project delivery. Requires substantial monitoring or data management experience and a degree in a health-related field. Drive team performance, resource planning, and client pr...

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...

Join Parexel as a Clinical Research Associate I in Bengaluru, India. You will manage site start-up, initiation, and close-out, ensuring patient safety across global projects. Ideal for candidates with substantial start-up experience and a degree in life sciences or nursing. Travel to investigator...

Seeking a skilled **Workday Integration / Extend Developer** in Bengaluru, India. You will architect, build, and deploy integrations using EIB, Studio, BIRT, and Core Connectors, with a focus on Workday Extend and Orchestrations. Requires 3+ years of hands-on experience, Workday Integration Certi...

Lead cross-functional clinical trial teams in Bengaluru to deliver patient-focused studies and accelerate treatments to market. This role requires project management skills, a science degree, and strong English proficiency. Enjoy a supportive, flexible environment with diverse projects and clear ...

Lead our Statistical Programming team in Hyderabad, Bengaluru, or Mumbai. You will manage project deliverables and a skilled team in diverse therapeutic areas, ensuring quality and efficiency in clinical data analysis. We offer flexible work, career growth, and a supportive, inclusive environment...

Join Parexel as a Clinical Research Associate II in Bengaluru. You will be integral to global clinical trials, ensuring patient safety and managing site start-up activities. We seek a degree-qualified professional with substantial start-up experience and strong problem-solving skills. Enjoy a sup...

Lead a clinical operations team in Bengaluru, ensuring high-quality, on-time project delivery. Utilize your substantial clinical research experience to manage, resource, and develop professionals. Drive project success through oversight, consultation, and client liaison in a dynamic CRO environment.

Seeking a Site Contract Associate II in Bengaluru to manage clinical trial site agreements. You will draft, negotiate, and finalize contracts, ensuring compliance and protecting client interests. The role requires 2-5 years of CRO experience, strong legal/analytical skills, and fluency in English.