Clinical Research Coordinator Job in Chandigarh at GastroLab India Private Limited
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Clinical Research Coordinator


Start date
Starts Immediately
Apply By
2 Aug' 21
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About GastroLab India Private Limited
GastroLab India Private Limited is a state-of-the-art start-up company set to revolutionize the way gastroenterologists & individuals approach and manage GI health. Our purpose is to bridge the gap in gastroenterology diagnostics and serve the unmet needs which can enable evidence-based management of the symptoms and condition.

Utilizing advances made in technology from the brightest minds around the world. We are making early and non-invasive health screening more accessible, affordable, and actionable for Indians everywhere. We are a start-up organization, self-funded, and work in close collaboration with innovative healthcare companies.
Activity on Internshala
Hiring since October 2019
22 opportunities posted
2 candidates hired
About the job
Key responsibilities:

1. Work on facilitating and coordinating the daily clinical trial activities while playing a critical role in the conduct of the study
2. Schedule 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 requirements
11. Assists 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 maintain records and other documentation of training
12. Maintain subject screening logs and protocol deviation logs
13. Maintain an Excel sheet for tracking updates to the database of all subjects enrolled in clinical trials
14. Coordinate and facilitate monitoring and auditing visits and notify appropriate institutional officials of external audits
15. Collaborate with PI and institutions to respond to any audit findings and implement approved recommendations
16. Complete documentation on each study visit that is used to track all study-related activities so that time, effort, and materials can be accounted for on a monthly basis
Skill(s) required
MS-Office Biology MS-Excel Bioinformatics English Proficiency (Spoken) English Proficiency (Written)
Learn these skills on Internshala Trainings
Who can apply

1. Those who are from Chandigarh and neighboring cities

2. Possesses a thorough knowledge of the informed consent process and a thorough understanding of the study protocol in order to be able to answer all questions pertaining to the study posed during the informed consent process

3. Computer competency, including proficiency in Microsoft Word, Excel, and PowerPoint

4. A postgraduate degree in a related field would be preferred or equivalent combination of education and experience

5. Familiarity with community research-based principles

6. Excellent facilitation skills

7. Excellent communication and interpersonal skills


Annual CTC: 3 LPA

Annual CTC breakup:

1. Fixed pay: 2.4 LPA

2. Variable pay: 0.6 LPA

Number of openings

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