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Showing posts with the label Parexel Jobs

Aurobindo Pharma FRD Internship 2026 for M.Pharm Candidates | ₹12,000 Stipend | Apply Before 21 August

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Aurobindo Pharma FRD Internship 2026 for M.Pharm Candidates | ₹12,000 Monthly Stipend (Aurobindo Pharma FRD Internship 2026) Introduction Aurobindo Pharma has announced an excellent internship opportunity for M.Pharm graduates who are looking to build a strong foundation in Pharmaceutical Research & Development (R&D) and Formulation Research & Development (FRD). This internship program offers hands-on exposure to pharmaceutical formulation activities, industry practices, regulatory guidelines, and research processes within one of India's leading pharmaceutical organizations. Candidates interested in pharmaceutical formulation development, drug product research, quality-focused development processes, and industrial exposure can use this internship as a stepping stone toward long-term careers in pharmaceutical R&D, formulation development, regulatory affairs, and related domains. The internship is based in Hyderabad and offers a monthly stipend along with practica...

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Parexel Hiring Regulatory Affairs Associate in India | Hyderabad, Bengaluru & Remote Opportunities for Regulatory Professionals

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Parexel Hiring Regulatory Affairs Associate in India | Hyderabad, Bengaluru & Remote Opportunities (Parexel Hiring Regulatory Affairs Associate in India) Introduction Regulatory Affairs continues to be one of the most important and rapidly growing functions within the pharmaceutical and life sciences industry. Professionals with expertise in regulatory submissions, CMC documentation, lifecycle management, and global regulatory compliance are increasingly in demand across pharmaceutical companies, CROs, and biotechnology organizations. Parexel, a globally recognized clinical research and regulatory consulting organization, has announced a new opportunity for the position of Regulatory Affairs Associate in India. The role is available in Hyderabad, Bengaluru, and remote work locations, offering experienced regulatory professionals an opportunity to contribute to post-approval regulatory activities, CMC lifecycle management, regulatory impact assessments, and European regulatory pr...

Parexel Hiring Patient Safety Associate I in Mohali 2026 | Pharmacovigilance Jobs for Freshers

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Parexel Hiring Patient Safety Associate I in Mohali 2026 | Pharmacovigilance Career Opportunity (Parexel Hiring Patient Safety Associate I in Mohali) Introduction If you are looking to start your career in pharmacovigilance and drug safety, this opportunity from Parexel is highly valuable. The company is hiring for the role of Patient Safety Associate I in Mohali, India, which is ideal for freshers and early-career professionals in pharmacy and life sciences. With the growing demand for drug safety professionals in 2026, roles like Patient Safety Associate are becoming one of the best entry points into the clinical research and pharmacovigilance industry. This job provides hands-on experience in ICSR processing, MedDRA coding, safety reporting, and global regulatory compliance. About The Company Parexel is a globally recognized Contract Research Organization (CRO) that provides clinical research, consulting, and regulatory services to pharmaceutical, biotechnology, and medical...

"Parexel Hiring Document Specialist I (Remote India) 2026 | Medical Writing & Regulatory Publishing Jobs"

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Parexel Hiring Document Specialist I – Remote Jobs in India (2026) Parexel Hiring Document Specialist I (Remote India) Introduction Global CRO companies are continuously expanding their operations in India, creating strong career opportunities in medical writing, regulatory publishing, and clinical documentation. Parexel, one of the world’s leading biopharmaceutical services organizations, is currently hiring for the position of Document Specialist I under its Medical Writing Support team. This is a full-time remote opportunity for candidates based in Mumbai, Hyderabad, Bengaluru, Chandigarh, and other Indian locations. If you have experience in clinical document compilation, publishing, CSR formatting, and regulatory submission support, this role offers excellent exposure to global clinical trials and regulatory deliverables. About The Company Parexel is a globally recognized Contract Research Organization (CRO) headquartered in Durham, North Carolina, USA. The company was found...

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