hireejobs
Register for Job
Hyderabad Jobs
Banglore Jobs
Chennai Jobs
Delhi Jobs
Ahmedabad Jobs
Mumbai Jobs
Pune Jobs
Vijayawada Jobs
Gurgaon Jobs
Noida Jobs
Oil & Gas Jobs
Banking Jobs
Construction Jobs
Top Management Jobs
IT - Software Jobs
Medical Healthcare Jobs
Purchase / Logistics Jobs
Sales
Ajax Jobs
Designing Jobs
ASP .NET Jobs
Java Jobs
MySQL Jobs
Sap hr Jobs
Software Testing Jobs
Html Jobs
IT Jobs
Logistics Jobs
Customer Service Jobs
Airport Jobs
Banking Jobs
Driver Jobs
Part Time Jobs
Civil Engineering Jobs
Accountant Jobs
Safety Officer Jobs
Nursing Jobs
Civil Engineering Jobs
Hospitality Jobs
Part Time Jobs
Security Jobs
Finance Jobs
Marketing Jobs
Shipping Jobs
Real Estate Jobs
Telecom Jobs

Project Manager - Clinical Trials

1.00 to 2.00 Years   Hyderabad   06 Jan, 2022
Jeevan Scientific Technology Limited
Job LocationHyderabad
EducationNot Mentioned
SalaryNot Disclosed
IndustryRecruitment Services
Functional AreaEngineering Design / Construction
EmploymentTypeFull-time

Job Description

JOB RESPONSIBILITIES:

  • Prepare project plan as per the project timelines, budget and deliverables. Complete the assigned project in Qualitative, cost effective and time bound manner.
  • Develop the contract and budget for clinical trial projects.
  • Conduct feasibility studies.
  • Track timelines, milestones and budget requirements for assigned projects
  • Coordinate for the required regulatory submission and approvals for the conduct of the study and CTRI registration.
  • Allocate CTLs/CRAs to clinical trial projects.
  • System enhancement in terms of developing appropriate study tools and tracking system
  • Assist new CTLs/CRAs in identifying and developing investigators for assigned studies.
  • Co-ordinate planning and conduct of clinical trial projects in liaison with CTLs/CRAs and other interdepartmental team members.
  • Assist in selection of the sites in conjunction with sponsor and lambda and recommend site assignments.
  • Provide protocol specific training to the CTLs/CRAs including therapeutic expertise, CRF conventions, study procedures and SOPs
  • Supervise activities of the CTLs/CRAs including the scheduling of monitoring visits, other activities associated with the project (e.g. review of visit reports for completeness and accuracy, assisting monitors with site problems etc and time accountability for the project.
  • Conduct quality control and co-monitoring visits with CTLs/CRAs to ensure quality and compliance with SOPs, GCP and project requirements.
  • Assist and guide CTLs/CRAs in conducting pre study, initiation, interim and close out monitoring visits as required.
  • Review and approve payments to the study site and vendors.
  • Prepare reports and updates for sponsor.
  • Ensure effective communication between stake holders and all project team members.
  • Guide the software team in developing e-CRF.
  • Identify and screen newer sites and PIs.
  • Identify the improvement areas in project management team
  • Create database of new PIs and sites.
,

Keyskills :
visitcorporate liaisoncrojstlcustomer relationscrfeffective communicationreportingjavatrialscost effectivegcpdeliveryclinical trialstrainingquality controlproject managementcontrolsoftwareclinical trial

APPLY NOW

Project Manager - Clinical Trials Related Jobs

© 2019 Hireejobs All Rights Reserved