Department :Trial Data Management Are you experienced in Clinical Data Management? Do you have a strong background in data handling and oversight? We are
Job Title:Lead Data Facilitation Programmer Department : CDS GBS Are you passionate about quality and simplification? Do you want to build quality within
Department :Global Safety. Does your motivation come from challenges and working in a dynamic environment? Do you thrive in a working environment where close
Department : Clinical Medical Regulatory (CMR) Do you want to be a part of a high performing team in Novo Nordisk that plays a critical role in driving the
Full-time Company DescriptionAbout m360 Research (m360 Research is a wholly owned subsidiary of M3): m360 Research is a full-service market research agency
Full-timeShift: DayTravel Requirements: 50% of the timeEmployee Type: EmployeeGlobal Job Level (HCM): Professional 1 (5) Company DescriptionAt Intuitive, we
Additional Locations:India:Haryana, Gurgaon Diversity : Innovation : Caring : Global Collaboration : Winning Spirit : High Performance At Boston Scientific,
Dear Candidate, Greeting form White Horse Manpower Consultancy P ltd!Required Candidates Currently Located In Bangalore Hiring for TOP BPO Leading Healthcare
SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and
Full-timeDepartment: ICSR Management Company DescriptionWe are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider
Full-timeDepartment: ICSR Management Company DescriptionWe are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider
Full-timeDepartment: ICSR Management Company DescriptionWe are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider
Relocation Assistance Offered Within Country 158505 : Mumbai, Maharashtra, India Who We Are Colgate:Palmolive Company is a caring, innovative growth company
1. FSE **NOVO NORDISK SCRA** **DEPARTMENT: Clinical/Medical** **JOB TITLE: Clinical Research Associate** **REPORTS TO: ICON DOCS Operations Manager** **SECTION
Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services New Associate
Full-time Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A
Work Mode : Hybrid Location: Gurugram Summary: As an individual contributor, the function of the Associate Regulatory Affairs Specialist is to support the
Full-time Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A
Full-time Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A
Regulatory Affairs Associate (GPR & Reg Ops) Full-timeJob Family: Regulatory AffairsSub Job Family: DocumentationPreferred type of working: