SIRO Clinpharm Hiring Principal Medical Writer Dear Connections, We have openings for Regulatory Medical Writing role for Principal & above level. Responsibilities Minimum 6+ years

IQVIA is hiring for Associate Clinical Lead roles Seeking for candidate between 5-10 Years experienced Clinical Research Associate background with strong Onsite Monitoring Experiences Skills:

Qinecsa India Hiring for Aggregate Reporting Role Years of exp: min 3+Years (Relevant exp in Aggregate Reporting PSUR PEBRER)Job Location: MysoreNotice Period: Immediate to 60

CDSCO Hiring for Pharmacovigilance Job positions

Novartis Hiring Medical Safety Writer – Aggregate Reports Your responsibilities include, but are not limited to: Lead preparation of global periodic safety reports for newly

Lilly Hiring for Regulatory Writers Skillset: Protocol Writing, CSRs, Submission Documents, IBs Share your profiles at chaki_sucharita@lilly.com

Quanticate Hiring Senior Pharmacovigilance Scientist Roles and Responsibilities Case Processing and Reporting: Manage the receipt and processing of cases (spontaneous, literature and clinical) in compliance

Springer Nature Hiring Scientific and Medical writer Experience: 1.5 Years+ experience in the Life Science domain. Qualification: B.Pharm, M.Pharm, M.Sc. (Biotechnology, Lifesciences), Ph.D (Pharma/ Lifesciences),

Haleon Hiring for Scientist Pharmacovigilance Single Case Processing Key Responsibilities : Serve a Haleon PV Ops, Single Case Processing global safety database SME contributing to

Quanticate is Hiring for Clinical Data Management (CDM) professional 6+ years of experience We are currently looking for a Lead Clinical Data Manager II to