Clinical Trials Jobs in Hyderabad
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Search Results - Clinical Trials Jobs in Hyderabad
Imaging Endpoints-Hyderabad
that are passionate in their desire to assist us in our mission to customize each clinical trial's imaging to optimize the opportunity to demonstrate efficacy.
Imaging Endpoints is based in Scottsdale, Arizona, with offices in Cambridge, Massachusetts; London, UK...
Signant Health-Hyderabad
About Signant Health
At Signant Health, we help bring life-changing treatments to patients faster. We are a global evidence generation company that supports clinical trials with smart technology, scientific expertise, and hands-on operational...
Imaging Endpoints-Hyderabad
that are passionate in their desire to assist us in our mission to customize each clinical trial’s imaging to optimize the opportunity to demonstrate efficacy.
Imaging Endpoints is based in Scottsdale, Arizona, with offices in Cambridge, Massachusetts; London, UK...
Bristol Myers Squibb-Hyderabad
centralized clinical trial payment operations including Ende to End PO management and Invoice/payment management across CROs, sites, labs, IRBs/ECs, and other vendors.
• Ensure compliance validation (budget, PO match, study match, vendor match...
foundit.in -
Ocugen India Pvt Ltd-Hyderabad
clinical data management experience in pharmaceutical development or CRO environment.
• Experience with clinical trials.
• Experience with CRFs, and in the development process of EDC databases, IRT systems and diary applications for data collection...
Latinum HR Solutions-Hyderabad
a Statistical Programmer – Clinical Data for a leading Pharma/Biotech organization. This role plays a key part in supporting clinical trials, regulatory submissions, and integrated analyses while ensuring high-quality statistical programming deliverables across...
Excelra-Hyderabad
Key Responsibilities
• Aid in the planning and writing of biomarker statistical analysis plans in the lead-up to clinical trials.
• Run and develop statistical models—such as random effects, mixed effects, and MMRM models—on biomarker data once...
SIRO-Hyderabad
Key Accountabilities:
• Create eCRF specifications, design, develop and unit test and functionally validate clinical trial setup process
• Create edit check specifications and program or modify checks at study level within EDC
• Setup different...
Latinum HR Solutions-Hyderabad
a Statistical Programmer – Clinical Data for a leading Pharma/Biotech organization. This role plays a key part in supporting clinical trials, regulatory submissions, and integrated analyses while ensuring high-quality statistical programming deliverables across...
Imaging Endpoints-Hyderabad
that are passionate in their desire to assist us in our mission to customize each clinical trial's imaging to optimize the opportunity to demonstrate efficacy.
Imaging Endpoints is based in Scottsdale, Arizona, with offices in Cambridge, Massachusetts; London, UK...
Youlabs.ai-Hyderabad
Strong leadership and mentoring skills, with a track record of managing clinical teams
• Experience in medical research, clinical trials, or the development of treatment protocols specific to endocrine disorders
• Exposure to technology and innovation...
Valos Srl-Hyderabad
Responsibilities
Create ADAM and TFLs for clinical studies
Apply advanced statistical methodologies to clinical trials and RWE studies
Contribute to the development of Statistical Analysis Plans (SAPs) and study reports
Collaborate closely with cross-functional...
Qinecsa Solutions-Hyderabad
Registration
Experience: 1 - 3 years in Pharmacovigilance
Primary Responsibilities
As a medical reviewer
• Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports
• Determine...
CloudLabs Inc-India
benefits, industry leading training.
• Opportunity to work remotely is available.
Experience Required: Medidata Rave, Custom Function Expert, Clinical Data Management.
Minimum 2-3 years of relevant experience as Medidata Rave EDC programmer and strong...
Ocugen India Pvt Ltd-Hyderabad
and leading cross‐functional communication.
• Proficiency in SAS (required).
• Strong understanding of clinical trial methodologies and statistical modeling.
• Experience with CDISC standards (SDTM, ADaM) and regulatory expectations.
• Excellent verbal...
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