Clinical Research Coordination Jobs in Bhubaneswar - GastroLab India Private Limited
Job Description
About the internship
Selected intern's day-to-day responsibilities include:
1. Work on facilitating and coordinating the daily clinical trial activities while playing a critical role in the conduct of the study
2. Schedule and study subject appointments and serve as the patient liaison to the PI and other participating physicians
3. Review and comprehend each assigned protocol, including study proceedings and timelines
4. Work closely with the PI & CRC participants in an integral way in the informed consent process by communicating clearly with potential study subjects about protocol
5. Coordinate approval of new study agreements and contracts
6. Coordinate and attend sponsor site selection visits, routine monitoring visits, and study close-out visits
7. Complete case report forms and extract data from patient files (source documents) in a timely manner
8. Respond to data clarification requests in a timely manner
9. Attend investigator meetings requiring travel and report pertinent information back to research team members
10. Coordinate with the departments to help ensure that clinical research and related activities are performed in accordance with protocol, SOP, GCP, and applicable regulatory
11. Assist the PI in the development of materials and tools necessary to appropriately train individuals involved in the conduct of the study, like study protocol requirements, schedule of visits, execution of research plan, and maintaining records and other documentation of training
1. Work on facilitating and coordinating the daily clinical trial activities while playing a critical role in the conduct of the study
2. Schedule and study subject appointments and serve as the patient liaison to the PI and other participating physicians
3. Review and comprehend each assigned protocol, including study proceedings and timelines
4. Work closely with the PI & CRC participants in an integral way in the informed consent process by communicating clearly with potential study subjects about protocol
5. Coordinate approval of new study agreements and contracts
6. Coordinate and attend sponsor site selection visits, routine monitoring visits, and study close-out visits
7. Complete case report forms and extract data from patient files (source documents) in a timely manner
8. Respond to data clarification requests in a timely manner
9. Attend investigator meetings requiring travel and report pertinent information back to research team members
10. Coordinate with the departments to help ensure that clinical research and related activities are performed in accordance with protocol, SOP, GCP, and applicable regulatory
11. Assist the PI in the development of materials and tools necessary to appropriately train individuals involved in the conduct of the study, like study protocol requirements, schedule of visits, execution of research plan, and maintaining records and other documentation of training
Skill(s) required
Who can apply
Only those candidates can apply who:
1. are available for full time (in-office) internship
4. are from Bhubaneswar, Chennai, Cuttack, Delhi, Indore, Kolkata, Lucknow, Thiruvananthapuram, Mumbai, Vellore and neighboring cities
5. have relevant skills and interests
Number of openings
10
Job Particulars
Role hr admin
Education Diploma, B.Com, M.Com, BBA/BBM, BCA, BE/B.Tech, MBA/PGDM, BSc, MCA, ME/M.Tech, MS, MSc, PG Diploma, 12th Pass (HSE)
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeInternship / Projects
Job Id1878228
Job Category Diploma , Recruitment
Locality Address
State Orissa
Country India
About Company
GastroLab India Private Limited
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