Clinical Associate Hyderabad
We have 35 ads for keyword clinical associate hyderabad
(0.000 seconds)YP-572 | Quality Assurance Associate, Print Quality Assurance
Description The Quality Assurance Associate will quickly analyze print book file quality and make decisions based on specifications and instructions. The QA
Quality Assurance Associate, Print Quality Assurance - [Z-433]
Description The Quality Assurance Associate will quickly analyze print book file quality and make decisions based on specifications and instructions. The QA
MSAT Associate : Upstream
/2024/04/23/jobs-33226025.jpg)
Full-timeJob Family: Research & DevelopmentSub Job Family: Upstream R&D - BiosimilarPreferred type of working: On-PremiseYears of Experience: 6 -
Research Associate - Mass Spectrometry
/2024/04/08/jobs-33219972.jpg)
Full-timeJob Family: Research & DevelopmentSub Job Family: Formulation R&D - BiosimilarPreferred type of working: On-PremiseYears of Experience: 1 -
Analyst III,R Global Process Owner - [Z945]
Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is
[OKD-779] Senior Clinical Data Associate
SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and
Senior Pharmacovigilance Associate/PV Associate (experienced Immediate joiners required for hybrid work)
/2024/03/25/jobs-33212909.jpg)
Full-timeDepartment: ICSR Management Company DescriptionWe are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider
Regulatory Affairs Associate (GPR & Reg Ops)
/2024/03/14/jobs-33208195.jpg)
Regulatory Affairs Associate (GPR & Reg Ops) Full-timeJob Family: Regulatory AffairsSub Job Family: DocumentationPreferred type of working:
Regulatory Affairs Associate (GPR & Reg Ops)
/2024/03/04/jobs-33203760.jpg)
Regulatory Affairs Associate (GPR & Reg Ops) Full-timeJob Family: Regulatory AffairsSub Job Family: DocumentationPreferred type of working:
MSAT Associate : Upstream
/2024/03/04/jobs-33203761.jpg)
Full-timeJob Family: Research & DevelopmentSub Job Family: Upstream R&D - BiosimilarPreferred type of working: On-PremiseYears of Experience: 7 -
Research Associate - Mass Spectrometry
/2024/02/21/jobs-33197687.jpg)
Full-timeJob Family: Research & DevelopmentSub Job Family: Advanced Characterisation TechniquePreferred type of working: On-PremiseYears of Experience: 3 -
Research Associate - Drug Device engineer
/2024/02/21/jobs-33197695.jpg)
Full-timeJob Family: Research & DevelopmentSub Job Family: R&D - GeneralBusiness unit: Biologics Company DescriptionCompany Description Dr. Reddy’s
QA Associate
/2024/02/16/jobs-33195387.jpg)
Full-timeJob Family: QualitySub Job Family: Quality GeneralYears of Experience: 5 - 7Business unit: Biologics Company DescriptionDr. Reddy’s Laboratories
QA Associate
/2024/02/14/jobs-33194300.jpg)
Full-timeJob Family: QualitySub Job Family: Quality GeneralYears of Experience: 5 - 7Business unit: Biologics Company DescriptionDr. Reddy’s Laboratories
QC Associate
/2024/02/12/jobs-33193559.jpg)
Full-timeJob Family: QualitySub Job Family: Quality GeneralYears of Experience: 5 - 7Business unit: Biologics Company DescriptionDr. Reddy’s Laboratories
QA Associate
/2024/02/12/jobs-33193565.jpg)
Full-timeJob Family: QualitySub Job Family: Quality GeneralYears of Experience: 5 - 7Business unit: Biologics Company DescriptionDr. Reddy’s Laboratories
CRA Manager
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
U-912 Senior Virtualization Engineer
Remote: Hybrid Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol
Clinical Project Manager | VMP349
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
Catalog Associate - Spanish, KCQ F619
Description Responsibilities: - The primary responsibility of the role is to perform analysis, quality checks on digital content of the e-book and to identify