Novartis Project Clinical Research Coordinator Recruitment at ILBS

Clinical Research Coordinator Job at ILBS – Applications Invited

Clinical Research Coordinator Job at ILBS – Applications Invited. Life Sciences candidates apply for Research Associate & Senior Research Fellow jobs at ILBS – Institute of Liver and Biliary Sciences. Check details on the same below:

This job expires in :

INTERVIEW FOR THE POST OF ‘CLINICAL RESEARCH COORDINATOR’
UNDER NOVARTIS PROJECT

Position: Clinical Research Coordinator

No. of opening: 01

Funding agency: Novartis Pharmaceuticals

Project duration: 3 months

Age Limit: 35 years

How to Apply:

1. Interested candidates who fulfil the mentioned qualifications/eligibility criteria may fill up
   the prescribed application form and forward it to [email protected] through email by 25th July 2021, 5:00 pm.
2. The effective date for reckoning the requisite qualification, experience and the upper age limit will be 30.06.2021.
3. Only shortlisted candidates will be called for written test/interview/skill test in the
   Institute. The shortlisted candidates will be required to bring all their photocopies of
   degree/certificate/diploma/testimonials along with their printed application form.
4. No TA/DA will be provided.
5. The extension can be given based on the performance of the candidate and sustainability of the project or availability of funds.

Remuneration: Rs 35,000/- (lump sum)

Essential: Master’s in Clinical

Research/Clinical Trials or Post Graduate Diploma in Clinical Research/Clinical Trial with 2 years of experience in handling global Clinical Trials post qualification.

Job description:

Key Responsibilities:

➢ Assist in the process of administering the informed consent to the potential study subjects and discussing in detail with them, the patient information sheet under the supervision of the investigator.
➢ Assist in ensuring the fulfilment of all the inclusion and exclusion criteria.
➢ Follow up with the site team for timely completion of the Source Documents and ensure that all the relevant information required in the Case Record Forms is present in the source
documents.
➢ Complete the EDC within the required timeline.
➢ Compile and update the Trial Master File.
➢ Maintain all the study related logs screening, enrollment and other communication logs, including forwarding all relevant logs to CRO/Sponsor in a timely manner.
➢ Archiving of trial documentation and correspondence.
➢ Interacting with Site/PIs & other study team members on regular basis, discuss potential issues and suggest corrective action.

See Notification Below

 

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