ROLE SUMMARY As part of the Clinical Data Sciences (CDS) group, an integral delivery unit within the Global Biometrics and Data Management (GBDM) organization,
Job Title: Associate Director - Statistical Programming Career Level - E Introduction to Role: Are you a goal-oriented Statistical Programmer looking for a new
Full-time Company DescriptionAbout m360 Research: m360 Research is a full-service market research agency specializing in the healthcare space. Our proprietary
Full-time Company DescriptionAbout m360 Research: m360 Research is a full-service market research agency specializing in the healthcare space. Our proprietary
Department: Data Systems and Automation, Clinical and Data Science (CDS) GBS Does your motivation come from challenges and working in a dynamic environment? Do
- Represent AbbVie Medical Affairs as subject matter expert Oncology and territory, provide scientific and technical leadership to ensure professional and
Department : Regions and operations, Global Medical Affairs Are you a life science/research graduate interested in medical writing? Do you enjoy collaborating
Work Mode : Hybrid Location: Gurugram Summary: As an individual contributor, the function of the Associate Regulatory Affairs Specialist is to support the
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
Remote: Hybrid Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol
Department:Centralised Monitoring Unit, CDS GBS : Bangalore Are you passionate about what you are doing? Do you want to build excellence within processes in
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
Department:Centralised Monitoring Unit, CDS GBS : Bangalore Job Level:6 Are you passionate about what you are doing? Do you want to build excellence within
Job Role's:- 1) Associate Project Manager (APM) exp:- 5 to 9 Years 2) Clinical Project Manager (PM) exp:- 9 to 15 Years Main Duties: · Management of one or
Catawba Research India is looking for an organized, flexible Clinical Research Associate to oversee clinical trials. Qualification: Bachelor’s Degree OR
We’re looking for people who are determined to make life better for people around the world. Clinical Trial Registry Writer Associate Level - Position title
No Relocation Assistance Offered 154640 : Mumbai, Maharashtra, India Li:Onsite About Colgate:Palmolive: Do you want to come to work with a smile and leave with
Work Mode : Hybrid Location: Gurugram Summary: As an individual contributor, the function of the Associate Regulatory Affairs Specialist is to support the
Department: Data Systems and Automation, Clinical and Data Science (CDS) GBS Job level: 5 Does your motivation come from challenges and working in a dynamic
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