Search Results: 2,073 vacancies
Summary
-This is a universal job description meant to capture some of the primary duties of this role that are common across functions or divisions. It is not intended to represent all of the specific responsibilities of the position. -Organizes, coordinates, monitors and ...
...of the LCTL/CTL, as assigned. Support the clinical protocol development process in collaboration... ...related documents; drive and/or supprt trial-related documents and processes.
development... ...procedures: attend CTT meetings, assist in report study progress and issues.
support...
...and the UK, our 700+ people support 245+ active projects and clinical trials across 50+ countries, with 400+ more staff across our social enterprises... ...and improving health outcomes worldwide. A Clinical Trial Assistant will work on trials testing new and existing drugs and will...
...Responsibilities
Support CRAs with the setup monitoring and closeout of clinical trials in accordance with Good Clinical Practice (GCP) ICH guidelines and company SOPs.
Assist in site qualification initiation and monitoring visits.
Review and track clinical trial documentation...
...seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of... ..., execution, and monitoring of clinical trials. The ideal candidate will have a strong understanding... ...queries.
Regulatory Compliance:
Assist in the preparation and submission of...
...and the UK, our 700+ people support 245+ active projects and clinical trials across 50+ countries, with 400+ more staff across our social enterprises... ...:
- Provide mentoring and guidance to early career staff, assisting them in their professional development and career progression....
...new data collection requirements in assigned studies and provide clinical input into the development of new and updated clinical Data... ...as well as 3rd party data collection methodologies) for assigned trials/therapy areas as needed.
Provide timely information for and support...
About the Role
Clinical Project Manager
Location – Hyderabad #LI Hybrid
About the Role:
This role is responsible to Lead and manage a multidisciplinary cross functional Clinical Trial Team (CTT) (medical writing, statistics, data management, monitoring partner,...
Summary
Responsible to execute clinical services and meet planned deliverables in line with defined roles and responsibilities agreed with... ...:
Support set-up and maintenance of information in Clinical Trial Management Systems (CTMS) and other systems as applicable, under...
Role: Senior Clinical SAS Programmer
Work Location: Hyderabad/Bangalore/Mumbai/Pune/Delhi/Kolkata
Experience Range: 5 to 12 years in... ...tables, listings and figures for various phases of clinical trials and across TA’s.
• Expertise in Base and Advance SAS programming...
...Model. Support documentation of appropriate oversight and tracking of TMF QC activities.
• Execute trial TMF QC activities in accordance with TCO portfolio and Clinical Operations Transition Decision Point (TDP) and Clinical Study Report (CSR) dates. Support CTTs with audit...
Summary
Responsible for Clinical execution and management of all aspects of assigned clinical studies (interventional and non-interventional... ...• Lead and manage a multidisciplinary cross functional Clinical Trial Team (CTT) (medical writing, statistics, data management,...
Rs 7 - 9 lakhs p.a.
• Deliver timely consistent, accurate and reproducible coding of clinical trial data using industry standard
coding dictionaries (MedDRA, WhoDrug) in line with global and therapeutic area guidelines.
• In collaboration with Global Data Manager, develop trial coding specifications...
...pharmacokinetics, pharmacodynamics, metabolism and clinical pharmacology in advancing the drug... ..., validations in support of clinical trials for biologics . Coordinate and monitor PK... ...assay development and qualification, used to assisting with LBA method troubleshooting across a...
...Associate Clinical Data Manager
SDC is a team of diversified professionals who deliver... ...data management on multiple studies
• Assist Clinical Data Managers or Project Managers... ...study documentation within the electronic Trial Master Files for multiple projects...
...About the role
“150! Clinical scientific experts, globally, are part of Global Drug Development (GDD) team, working to ensure clinical trial data and regulatory reports are of highest quality throughout the life cycle of each program, across all disease areas. Be part of...
...Position: Clinical Data Manager
Requirement: Immediate Joiner
Location: Hyderabad
Experience: 3 to 10 Years
Key Roles & Responsibilities... ...to leverage technologies like R Python & Julia in clinical trials.
Identify opportunities for AI & ML in clinical trials....
...talented people in the industry.
Senior Clinical Data Associate
Job Summary:
Performs... ...listing reviews within the
electronic Trial Master Files for multiple projects
•... ...resolution on multiple studies as
needed to assist lead Clinical Data Managers
• Performs...
...About the role
Clinical Data Scientist
Location – Hyderabad/ Mumbai
About the Role:
Provide timely and professional ongoing management of Data Management deliverables and of clinical trial data with respect to cost, quality and timelines for all assigned trials...
...JOb Role: Clinical Manager
Location: Pune/Hyd/Bangalore
JOB DESCRIPTION :
• Should be trained on SCM (Sunrise Clinical Manager) & Pharmacy Module (SMM)
• Should well versed with SCM Configuration Tools
• Should have build experience/expertise in Pharmacy (Generic...
