Regulatory Affairs Job at ClinChoice | Apply for the Senior Associate Role
ClinChoice, a global life sciences partner, is seeking a Senior Associate – Regulatory Affairs for a full-time position based in Bengaluru or Hyderabad. This Regulatory Affairs Job focuses on the operational aspects of regulatory submissions, particularly the technical processes of building, publishing, and archiving activities for assigned projects. Candidates must possess a Bachelor’s or Master’s degree in Pharmacy or Life Sciences and strong English skills. The Associate in this Pharmacy Job will ensure adherence to quality procedures, use document management and publishing platforms, and maintain regulatory compliance across the submission portfolio. The position is ideal for someone interested in a Regulatory Affairs Job with operational responsibilities.
- Job Post: Senior Associate – Regulatory Affairs
- Location: Bangalore
About ClinChoice
ClinChoice is a global partner specializing in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, and toxicology for leading pharmaceutical, medical device, and consumer care innovators. Interested candidates for the Regulatory Affairs Job should note that ClinChoice was established in 1995 and leverages its global delivery network across the US, UK, Asia, and India to provide expertise that accelerates clinical trials and delivers optimal strategies for product registration. The company is committed to maintaining local and global regulatory compliance through data-driven insights and cutting-edge solutions.
Requirements for the Regulatory Affairs Job
- Bachelor’s or Master’s degree in Pharmacy
- Strong English language skills, both written and verbal.
- Good interpersonal skills with excellent collaboration capabilities.
- Proactive and initiative-driven.
- Solution-oriented in approach.
Primary Responsibilities
- Responsible for building, publishing, and archiving activities, along with associated tasks for assigned regulatory submissions within agreed timelines.
- Adhere to quality procedures and standards related to submission publishing in thei Pharmacy Job
- Ensure the appropriate use of document management systems, publishing platforms, and validation tools through established working practices and quality-control steps to maintain regulatory compliance.
- Support other team members with submission workload when necessary, providing flexible support for the submission portfolio.
- Support global/local teams by completing tasks assigned by submission coordinators.
- Adhere to Pfizer compliance standards.
