Designation : Clinical Research Coordinator
Job Description : To help out the Investigators in recruiting patients for a given trial, by pre-identifying the potential patients and leveraging the existing database Performing the site management activities and the data cleaning activities for the assigned projects in accordance with our SOPs. A CRC who is appointed to some specific sites within the organization, is responsible for achieving and maintaining high site performance while ensuring the good Quality of the data which includes the relationship with the PI(s), collating Regulatory Documentation, handling qualification visits/audits initiated by Sponsors and/or CROs, performing site documentation verification, data collection, queries resolution and conduction site close outs.
Desired Profile: high level of coordination and organizational skills. Excellent interpersonal, site management and relationship building, verbal and written communication skills including excellent presentation skills. Able to take initiative and be autonomous good analytical skills Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail. Able to prioritize in completing assigned tasks.
Experience : 2 - 3 Years in this position
Industry Type : Pharma/ Biotech/Clinical Research
Role : Clinical Research Coordintator
Functional Area : Healthcare, Medical, R&D
Education : UG - B.Pharma - Pharmacy PG - M.Pharma - Pharmacy,M.Sc -Any Specialization
Designation : Project Manager
Job Description : The responsibility of a PM is as follows: Primary focus on exceeding enrolment goals, ensuring highest quality data, and ensuring our clients and sites have the best experience working with the Company Manage all aspects of assigned projects throughout the development project lifecycle including project scope, schedule, resources, quality, costs and change. Develop and maintain detailed project plan to include milestones, tasks, and target/actual dates of completion. Ability to effectively manage time, prioritize work, multi-task across many assignments - Manages day-to-day operational aspects of a project and scope. Revise project plans as appropriate as a result of approved changed requests. Prepare and submit project status reports to management. Manage study budget. Conduct regularly scheduled project status update meetings. Minimizes our exposure and risk on project. Ensures project documents are complete, current, and stored appropriately. Desired Profile: Excellent interpersonal, site management and relationship building, verbal and written communication skills including excellent presentation skills. must be willing to work in a team environment high level of coordination and organizational skills. must have the oratory skills required to address different departments of people involved in the project he is handling. strong ability to work with very little guidance/supervision with a proactive approach.
Experience: Extensive experience conducting study start up, very hands on 3-5 years of experience in the Pharmaceutical or CRO industry is REQUIRED in this position or similar positions Knowledge MS Office, Word, Excel, Access and Powerpoint, and MS Project Proven experience in developing complete project plans and managing budgets
Industry Type : Pharma/ Biotech/Clinical Research
Role : Project Manager
Functional Area : Healthcare, Medical, R&D
Education :PG - M.Pharma - UG - B.Pharma - Pharmacy,B.Sc - Any Specialization, Bio-Chemistry, Biology, Chemistry, Microbiology,MBBS - Medicine
Location : Bangalore
Only interested candidates with relevant experience can send their cv to hrclinical.dept@gmail.com
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