BSc & MSc Life Sciences CRA Job With Rs. 49,000 pm Pay at BRIC-THSTI – Apply Online

Clinical Research Associate Latest Jobs

RECRUITMENT NOTICE NO.: THS-C/RN/14/2025 Dated: 14th August 2025
RECRUITMENT NOTIFICATION

Educational Qualification and Experience required for the post:

Name of the post: Clinical Research Associate

Number of the post: 01

Name of the Project: Sepsis-related mortality in neonates in India: A multi-disciplinary, multi-institutional research program for context-specific solutions

Emoluments: Rs. 49,000/- + HRA

Age: 35 years

Minimum Educational Qualification and Experience

• Bachelor’s in Life Sciences with a minimum of three years of relevant clinical trial monitoring experience or clinical trial/study coordinator, or clinical trial/study associate experience.
OR
• Master’s degree/diploma, life sciences, pharmacy, public health, healthcare or other related discipline with a minimum of 2 years of relevant clinical trial monitoring experience or clinical trial/study coordinator, or clinical trial/study associate experience.
OR
• MBBS/ BDS/ BHMS/ BAMS/ BPT with a minimum of 2 years of relevant clinical trial monitoring or clinical trial/study coordinator, or clinical trial/study associate experience.

Job profile

The Clinical Research Associate (CRA) is responsible for overseeing clinical research sites to ensure adherence to study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements. This position involves conducting regular monitoring visits, supporting site operations, and maintaining data quality and compliance across all phases of the clinical trial lifecycle.

• Conduct site monitoring visits from initiation through closeout, ensuring trials are conducted in compliance with the study protocol, GCP guidelines, SOPs, and applicable regulatory requirements.
• Set up trial sites, ensuring that investigational products and essential trial supplies are delivered, stored, and documented appropriately.
• Perform quality checks and execute quality assurance process across clinical operations and clinical laboratories in accordance with GCP/GCLP standards.
• Provide training on protocols and trial procedures to site staff and maintain ongoing communication to support study execution and address issues.
• Support clinical staff through guidance and training as and when needed.
• Create, maintain, and submit all required documentation related to site management, monitoring visits, findings, and follow-up actions.
• Track and manage study progress, including regulatory and ethics submissions, patient recruitment and enrolment, CRF completion, and data query resolution.
• Verify data accuracy through source data/document verification to ensure consistency between CRFs and clinical records.
• Prepare detailed monitoring visit reports and contribute to the preparation and archiving of essential trial documents.
• Assess trial site compliance and escalate quality or protocol deviations to the Project Manager or Senior Leadership as appropriate.
• Collaborate with Clinical Portfolio Management and other internal departments on cross-functional initiatives and project requirements.

Skills

• Proficient in computer applications, with demonstrated expertise in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).
• Strong knowledge of ICH-GCP, GCLP, and regulatory guidelines.
• Excellent documentation, communication, and organizational skills.
• Ability to travel frequently to assigned trial sites.
• Detail-oriented with effective time management skills and ability to manage multiple tasks and priorities efficiently.

Date of walk-in interview: 28th August 2025

For posts mentioned above:

➢ Last date for receipt of online application for posts: 03 September 2025.
➢ The applications will be scrutinised/shortlisted and processed for further selection.

NOTE:

1. The candidates applying for the post of S.No. 1,2 & 3 must bring their latest resume, one set of photocopy of documents in support of their educational qualification and experience along with originals and a valid ID card for verification.

2. Candidates coming after the time slot mentioned will not be entertained.

3. All the candidates coming for written test/skill test/interview will be mandatorily required to deposit their mobile phone along with a valid Identity proof at the reception and the same will only be returned back on completion of the entire selection process.

GENERAL TERMS & CONDITIONS For Clinical Research Associate Latest Jobs

a) These are the short-term positions and extension will be granted subject to satisfactory performance of the incumbents and tenure of the project for which they are selected. Those appointed to these positions will not have any claim for regularization of their employment.
b) All educational, professional and technical qualification should be from a recognized Board/University.
c) The experience requirement specified above shall be the experience acquired after obtaining the minimum educational qualifications specified for the post. The candidates are required to satisfy themselves, before applying /appearing for the selection process, that they possess the minimum eligibility criteria as laid down in the recruitment advertisement. No query will be entertained with regard to the eligibility criteria.
d) Closing date of online application will be the CRUCIAL DATE for determining eligibility with regard to age, essential qualification, experience etc.
e) The age limit, qualification, experience and other requirements may be relaxed at the discretion of the competent authority, in case of candidates who are otherwise suitable.
f) Age and other relaxations for direct recruits and departmental candidates:

1. By five years for candidates belonging to SC/ST communities.

2. By three years for candidates belonging to OBC communities.

3. For Persons with Benchmark Disabilities (PwBD) falling under the following categories : (i) UR – ten years, (ii) OBC – 13 years, (iii) SC/ST – 15.

4. Age is relaxable for Central Government servants up to five years in accordance with the instructions or orders issued by the Central Government, from time to time.

5. Institute employees will get the age relaxation to the extent of the service rendered by them as on closing date of advertisement.

6. For Ex-servicemen up to the extent of service rendered in defence forces (Army, Navy & Air force) plus 3 years provided they have put in a minimum of 6 months attested service.
   g) All results/notifications will only be published on our website. Therefore, the candidates should essentially visit THSTI website regularly.
   h) All communications will only be made through email.
   i) In case a large number of applications are received, screening will be done to limit the number of candidates to those possessing higher/relevant qualification and experience.
   j) The no. of vacancy indicated above may change subject to the actual requirement at the time of Written test/skill test/interview.
   k) With regard to any provisions not covered in this notification, the bye laws of THSTI / Govt. of India rules/guidelines shall prevail.
   l) Canvassing wrong information in any form will be a disqualification.

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