6 Trial Management Jobs

As a Research Coordinator at Jothydev's Diabetes Research Centre, your role will involve assisting in trial management and site coordination, maintaining Trial Master Files (TMF) with proper documentation, and ensuring regulatory compliance. You will also be responsible for drug storage, dispensing, and accountability, as well as supporting patient enrollment and clinical trial material logistics. Additionally, you will schedule meetings, prepare agendas and minutes, demonstrating your technical and soft skills including knowledge of ICH-GCP guidelines, proficiency in Microsoft Office and clinical trial software, and strong organizational and communication abilities. Qualifications required ...

Company Description QREC Clinical Research LLP is a Contract Research Organisation with offices in Jaipur (India), Hyderabad (India), and Dubai (UAE). They offer comprehensive services to the healthcare industry, including clinical trials (Phase 3 & 4), REAL WORLD, observational studies, PMS, KAP surveys, investigator-initiated studies, medical writing, clinical data management, statistical analysis, and medico marketing globally. QREC has contributed significantly to the healthcare industry with over 450 brand plans, 162 REAL world studies, 9 global studies, and numerous other projects. Their extensive database includes 45,000+ doctors, 810,000+ patients, and 180+ publications, and they hav...

As a Core member of the Clinical Trial Team (CTT) at Novartis Healthcare Private Limited in Hyderabad, India, your role will involve independently managing all clinical vendor-related aspects of global clinical trials. You will be responsible for ensuring the delivery of study outcomes within schedule, budget, quality/compliance, and performance standards. Your proactive approach will involve managing vendor-related risks and potential issues, implementing the global vendor strategy, and escalating vendor issues to the VSM or Vendor Alliance Lead (VAL) as needed. Additionally, you will keep the Trial Lead and Vendor Program Strategy Directors informed about vendor risks and issues while over...

Summary Core member of the Clinical Trial Team (CTT), independently managing all clinical vendor-related aspects of global clinical trial(s) to deliver study outcomes within schedule, budget, quality/compliance and performance standards. Proactively manages vendor-related risks and potential issues. Implements global vendor strategy and if required, escalates vendor issues to the VSM or Vendor Alliance Lead (VAL) while keeping Trial Lead and Vendor Program Strategy Directors informed about vendor risks and issues. Oversees vendor compliance at study level. About The Role Major accountabilities: Close interaction and collaboration with study Trial Lead and study team members during study life...

Agronomists • Field Research and Trial Management: Plan, execute, and monitor field trials, demonstrations, and surveys to assess the effectiveness of fertilizers (e.g., TSP, TSP+). Gather accurate data and interpret results for products efficacy and adoption among farmers. • Farmer Engagement & Advisory: Provide advisory services, (based on recommendations given by State Agriculture department/State Universities/Research Institutes.) conducting training, and building trust among farmers to ensure effective product awareness/promotion. • Awareness Program: Work closely with farmer to provide TSP or any new product awareness among target demographics. • Stakeholder Relationship Management : M...

Trial Management (Initiation,Execution,Reporting) Identify trial locations/universities and initiate collaborations. Develop protocols, obtain approvals, and manage trial payments. Oversee execution through site visits and ensure protocol adherence. Required Candidate profile M.Sc. (Agronomy)/(Horticulture),related to agriculture research community. Min 2 yrs of exp,preferably in field operations/field researches as a Technical Officer,Field Officer,Field In-Charge.