BRIC-THSTI CDSA Recruitment 2025: Project Research Scientist (B.Pharm/Pharm.D/Medical) Jobs

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BRIC-THSTI Recruitment 2025: Project Research Scientist (B.Pharm/Pharm.D/Medical) & Data Entry Operator Jobs

BRIC-Translational Health Science and Technology Institute (THSTI)

RECRUITMENT NOTIFICATION: PROJECT POSITIONS AT CDSA CENTER

About THSTI and CDSA

Institute Overview
Institute Name	BRIC-Translational Health Science and Technology Institute (THSTI)
Parent Organization	Biotechnology Research and Innovation Council, Department of Biotechnology, Ministry of Science & Technology, Govt. of India
Location	NCR Biotech Science Cluster, 3rd Milestone, Faridabad – Gurugram Expressway, P.O. Box No. 04, Faridabad – 121001
Mission	To conduct innovative translational research and develop research collaborations to translate concepts into products for human health improvement
Associated Center	Clinical Development Services Agency (CDSA), a niche center established to facilitate affordable healthcare product development for public health diseases

Recruitment Summary

Key Information
Recruitment Notice No.	THS-C/RN/18/2025
Notification Date	02 September 2025
Application Last Date	22 September 2025
Mode of Application	Online

Available Vacancies

Sr. No.	Post Name	Number of Posts	Project Name	Emoluments	Max. Age
1	Project Research Scientist – I (Medical)	01	Early Intervention with Low Molecular Weight Heparin (Enoxaparin) for Prevention of Moderate to Severe Acute Pancreatitis: A Double-Blind Placebo Controlled Investigator Initiated Multicenter Randomised Trial	Rs. 67,000/- + HRA	40 years
2	Data Entry Operator	01	Early Intervention with Low Molecular Weight Heparin (Enoxaparin) for Prevention of Moderate to Severe Acute Pancreatitis: A Double-Blind Placebo Controlled Investigator Initiated Multicenter Randomised Trial	Up to Rs 29,000/-	35 years

Educational Qualifications & Experience

Post Name	Minimum Educational Qualification and Experience
Project Research Scientist – I (Medical)	Essential Qualification: Candidates must hold an MBBS, BDS, BVSC, BAMS, BHMS, BUMS, BSMS, BNYS, B.Sc. Nursing, BPT, B.Pharm, Pharm.D or equivalent degree from a recognized institution. Required Experience: A minimum of two years of post-qualification experience in clinical project management and/or clinical trial/study monitoring is essential. This experience should be gained in a recognized organization/institute such as a hospital, academic clinical trials unit, CRO, pharmaceutical, or medical device company.
Data Entry Operator	Option 1: A Graduate degree in any discipline combined with a computer diploma and 2 years’ experience in a reputed organization as a data entry operator/computer operator/assistant. OR Option 2: An Intermediate/ 12th pass with a computer diploma and 5 years’ experience in a reputed organization as a data entry operator/computer operator/assistant. Additional Requirement: Candidates must demonstrate a typing speed of not less than 15000 key depressions per hour through a speed test on computer.

Post Name

Minimum Educational Qualification and Experience

                    Project Research Scientist – I (Medical)
                    
                        Essential Qualification: Candidates must hold an MBBS, BDS, BVSC, BAMS, BHMS, BUMS, BSMS, BNYS, B.Sc. Nursing, BPT, B.Pharm, Pharm.D or equivalent degree from a recognized institution.
Required Experience: A minimum of two years of post-qualification experience in clinical project management and/or clinical trial/study monitoring is essential. This experience should be gained in a recognized organization/institute such as a hospital, academic clinical trials unit, CRO, pharmaceutical, or medical device company.

Data Entry Operator

Option 1: A Graduate degree in any discipline combined with a computer diploma and 2 years’ experience in a reputed organization as a data entry operator/computer operator/assistant.
OR
Option 2: An Intermediate/ 12th pass with a computer diploma and 5 years’ experience in a reputed organization as a data entry operator/computer operator/assistant.
Additional Requirement: Candidates must demonstrate a typing speed of not less than 15000 key depressions per hour through a speed test on computer.

Job Profile and Responsibilities

Post Name	Key Responsibilities
Project Research Scientist – I (Medical)	Responsible for overseeing clinical trial sites from initiation to closeout, ensuring full compliance with study protocols, ICH-GCP, applicable regulations, and internal SOPs. Conduct various monitoring visits (on-site and remote), including initiation, routine monitoring, and closeout activities. Ensure that all trial sites adhere strictly to regulatory, protocol, and GCP requirements. Execute risk-based monitoring and promptly escalate any site issues or protocol deviations. Verify informed consent processes and subject safety protocols are aligned with ethical standards. Monitor timelines for Adverse Event (AE) / Serious Adverse Event (SAE) reporting to ensure regulatory compliance and escalate delayed submissions to the pharmacovigilance team. Review source documents and Case Report Forms (CRFs) to verify data accuracy and consistency through Source Data Verification (SDV). Ensure appropriate management and meticulous documentation of the investigational product (IP). Maintain all essential trial documents in strict accordance with ICH GCP and local regulations. Prepare detailed monitoring visit reports and efficiently manage action items identified during visits. Provide support for regulatory and ethics submissions, patient recruitment efforts, and resolution of data queries. Offer comprehensive training to site personnel on study protocols, GCP, and Standard Operating Procedures (SOPs). Ensure timely delivery and proper handling of all study supplies and investigational product. Monitor quality metrics and assist in the implementation of Corrective and Preventive Actions (CAPA). Ensure site readiness for both internal and external audits and regulatory inspections.
Data Entry Operator	Primarily responsible for error-free data entry and efficient management of data within defined timelines. Maintain organized documentation and provide support with data filing, printing, or scanning as required. Participate actively in training sessions related to the utilization of electronic data capture (EDC) systems and study protocols. Assist in resolving data queries in close coordination with the site staff and central data management team. Support periodic quality checks and audits of entered data to ensure accuracy. Report any missing or unclear information to the data manager or site staff for timely clarification. Maintain up-to-date records of all entered data and ensure timely completion of data entry tasks. Review and meticulously verify data for accuracy, completeness, and consistency against source documents. Ensure strict data confidentiality and secure handling of patient information at all times.

Post Name

Key Responsibilities

                    Project Research Scientist – I (Medical)
                    
                        Responsible for overseeing clinical trial sites from initiation to closeout, ensuring full compliance with study protocols, ICH-GCP, applicable regulations, and internal SOPs.
Conduct various monitoring visits (on-site and remote), including initiation, routine monitoring, and closeout activities.
Ensure that all trial sites adhere strictly to regulatory, protocol, and GCP requirements.
Execute risk-based monitoring and promptly escalate any site issues or protocol deviations.
Verify informed consent processes and subject safety protocols are aligned with ethical standards.
Monitor timelines for Adverse Event (AE) / Serious Adverse Event (SAE) reporting to ensure regulatory compliance and escalate delayed submissions to the pharmacovigilance team.
Review source documents and Case Report Forms (CRFs) to verify data accuracy and consistency through Source Data Verification (SDV).
Ensure appropriate management and meticulous documentation of the investigational product (IP).
Maintain all essential trial documents in strict accordance with ICH GCP and local regulations.
Prepare detailed monitoring visit reports and efficiently manage action items identified during visits.
Provide support for regulatory and ethics submissions, patient recruitment efforts, and resolution of data queries.
Offer comprehensive training to site personnel on study protocols, GCP, and Standard Operating Procedures (SOPs).
Ensure timely delivery and proper handling of all study supplies and investigational product.
Monitor quality metrics and assist in the implementation of Corrective and Preventive Actions (CAPA).
Ensure site readiness for both internal and external audits and regulatory inspections.

                    
                

Data Entry Operator

Primarily responsible for error-free data entry and efficient management of data within defined timelines.
Maintain organized documentation and provide support with data filing, printing, or scanning as required.
Participate actively in training sessions related to the utilization of electronic data capture (EDC) systems and study protocols.
Assist in resolving data queries in close coordination with the site staff and central data management team.
Support periodic quality checks and audits of entered data to ensure accuracy.
Report any missing or unclear information to the data manager or site staff for timely clarification.
Maintain up-to-date records of all entered data and ensure timely completion of data entry tasks.
Review and meticulously verify data for accuracy, completeness, and consistency against source documents.
Ensure strict data confidentiality and secure handling of patient information at all times.

Required Skills

Post Name	Key Skills and Competencies
Project Research Scientist – I (Medical)	Proficiency in using clinical trial systems such as EDC (Electronic Data Capture), CTMS (Clinical Trial Management System), and eTMF (electronic Trial Master File) for tracking, documentation, and communication. Ability to maintain effective communication with investigators and site staff to ensure study success. Willingness and ability to travel frequently to assigned trial/study sites by eligible modes of travel. Strong collaboration skills for working with Clinical Portfolio Management on assigned projects and providing support to other internal departments. Proficiency 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. Detail-oriented approach with effective time management skills and the ability to manage multiple tasks and priorities efficiently.
Data Entry Operator	Ability to keep track of reports and provide efficient support in the extraction of data. Capable of assisting the data management team in any other data-related or clerical tasks as assigned. Prior experience in clinical data entry or working in a healthcare/research setting is highly desirable. Proficiency in Microsoft Office tools (Word, Excel); experience with data entry software or EDC systems is a definite advantage. Demonstrated good typing speed with high accuracy and meticulous attention to detail. Ability to work effectively under supervision and meet tight deadlines. Strong communication and organizational skills. Must exhibit a team-player attitude. Ability to model behavior and ethics in line with the CDSA Mission and Vision.

Post Name

Key Skills and Competencies

                    Project Research Scientist – I (Medical)
                    
                        Proficiency in using clinical trial systems such as EDC (Electronic Data Capture), CTMS (Clinical Trial Management System), and eTMF (electronic Trial Master File) for tracking, documentation, and communication.
Ability to maintain effective communication with investigators and site staff to ensure study success.
Willingness and ability to travel frequently to assigned trial/study sites by eligible modes of travel.
Strong collaboration skills for working with Clinical Portfolio Management on assigned projects and providing support to other internal departments.
Proficiency 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.
Detail-oriented approach with effective time management skills and the ability to manage multiple tasks and priorities efficiently.

                    
                

Data Entry Operator

Ability to keep track of reports and provide efficient support in the extraction of data.
Capable of assisting the data management team in any other data-related or clerical tasks as assigned.
Prior experience in clinical data entry or working in a healthcare/research setting is highly desirable.
Proficiency in Microsoft Office tools (Word, Excel); experience with data entry software or EDC systems is a definite advantage.
Demonstrated good typing speed with high accuracy and meticulous attention to detail.
Ability to work effectively under supervision and meet tight deadlines.
Strong communication and organizational skills.
Must exhibit a team-player attitude.
Ability to model behavior and ethics in line with the CDSA Mission and Vision.

Application Fee Details

Non-Refundable Application Fee
For Unreserved, OBC & EWS Candidates	For Project Research Scientist – I (Medical) (Sr. No. 1): Rs 590/- For Data Entry Operator (Sr. No. 2): Rs 236/-
For SC/ST/Women/PwBD Candidates	Rs 118/- (Applicable for both Sr. No. 1 & 2)
Payment Mode	Online Mode Only (Debit Card / Credit Card / Internet Banking/ UPI). Fee once paid is non-refundable.

General Terms & Conditions

Important General Information
These are short-term positions, and any extension will be granted solely based on the satisfactory performance of the incumbent and the tenure of the project. Appointed candidates will not have any claim for regularization of their employment. All educational, professional, and technical qualifications cited must be obtained from a recognized Board/University. The experience requirement specified must be experience acquired after obtaining the minimum educational qualifications for the respective post. The closing date of online application (22 September 2025) will be the CRUCIAL DATE for determining eligibility with regard to age, essential qualification, and experience. The age limit, qualification, experience, and other requirements may be relaxed at the discretion of the competent authority in cases of otherwise suitable candidates. Age and other relaxations are provided as per government norms for various categories: 5 years for SC/ST, 3 years for OBC, 10-15 years for Persons with Benchmark Disabilities (PwBD), up to 5 years for Central Government servants, age relaxation for Institute employees based on service rendered, and for Ex-servicemen. All results and notifications pertaining to this recruitment will be published only on the THSTI website. Candidates are advised to visit the website regularly. All official communications will be exclusively made through email. In the event of a large number of applications, screening will be conducted to shortlist candidates possessing higher/relevant qualifications and experience. The number of vacancies indicated may change subject to the actual requirement at the time of Written test/skill test/interview. With regard to any provisions not explicitly covered in this notification, the bye-laws of THSTI / Govt. of India rules/guidelines shall prevail. Providing wrong information or canvassing in any form will lead to disqualification of the candidature.

Important General Information

These are short-term positions, and any extension will be granted solely based on the satisfactory performance of the incumbent and the tenure of the project. Appointed candidates will not have any claim for regularization of their employment.
All educational, professional, and technical qualifications cited must be obtained from a recognized Board/University.
The experience requirement specified must be experience acquired after obtaining the minimum educational qualifications for the respective post.
The closing date of online application (22 September 2025) will be the CRUCIAL DATE for determining eligibility with regard to age, essential qualification, and experience.
The age limit, qualification, experience, and other requirements may be relaxed at the discretion of the competent authority in cases of otherwise suitable candidates.
Age and other relaxations are provided as per government norms for various categories: 5 years for SC/ST, 3 years for OBC, 10-15 years for Persons with Benchmark Disabilities (PwBD), up to 5 years for Central Government servants, age relaxation for Institute employees based on service rendered, and for Ex-servicemen.
All results and notifications pertaining to this recruitment will be published only on the THSTI website. Candidates are advised to visit the website regularly.
All official communications will be exclusively made through email.
In the event of a large number of applications, screening will be conducted to shortlist candidates possessing higher/relevant qualifications and experience.
The number of vacancies indicated may change subject to the actual requirement at the time of Written test/skill test/interview.
With regard to any provisions not explicitly covered in this notification, the bye-laws of THSTI / Govt. of India rules/guidelines shall prevail.
Providing wrong information or canvassing in any form will lead to disqualification of the candidature.

How to Apply Online

Application Procedure
Documents to Keep Handy Before Filling the Online Application (PDF format for all except photo/signature): A soft copy of your passport size photograph and signature (jpeg/jpg/png format). A comprehensive CV containing detailed information about qualifications, positions held, professional experience, and distinctions. Matriculation certificate (equivalent to 10th Standard) / Mark sheet. Intermediate certificate (equivalent to 12th Standard) / Mark sheet. Graduation/Diploma degree certificate / Mark sheet. Post-Graduation degree certificate & Mark sheet (if applicable). PhD degree/certificate (if applicable). Relevant experience certificates (if applicable). Caste / Disability certificate in the format prescribed by the Govt. of India, if applicable. Step-wise Online Application Process: The eligible and interested candidates must apply online through the Institute’s website. Applications submitted through any other mode will not be accepted. Follow the step-wise procedure: Step 1: Details of applicant – Provide your personal and contact details accurately. Step 2: Uploading of documents – Upload all the required documents in the specified formats. Step 3: Payment of application fee – Make the non-refundable application fee payment using Debit Card / Credit Card / Internet Banking / UPI. Please note that no correction or modification is possible once payment is made, and the fee will not be refunded. Upon successful submission, an auto-generated email containing the reference number will be sent to your registered email address. Keep this reference number for all future correspondence. Candidates are advised to keep a printout of the online application form for their records. It is crucial for candidates to ensure they fulfil all the eligibility criteria as stipulated in this advertisement. Failure to meet the criteria at any stage will lead to cancellation of candidature/termination. Incomplete applications will be summarily rejected, and no correspondence will be entertained regarding them. In case of any difficulty during the online application process, please send an e-mail to HR.CDSA@THSTI.RES.IN, attaching a screenshot of the error displayed.

Application Procedure

Documents to Keep Handy Before Filling the Online Application (PDF format for all except photo/signature):

A soft copy of your passport size photograph and signature (jpeg/jpg/png format).
A comprehensive CV containing detailed information about qualifications, positions held, professional experience, and distinctions.
Matriculation certificate (equivalent to 10th Standard) / Mark sheet.
Intermediate certificate (equivalent to 12th Standard) / Mark sheet.
Graduation/Diploma degree certificate / Mark sheet.
Post-Graduation degree certificate & Mark sheet (if applicable).
PhD degree/certificate (if applicable).
Relevant experience certificates (if applicable).
Caste / Disability certificate in the format prescribed by the Govt. of India, if applicable.

Step-wise Online Application Process:

The eligible and interested candidates must apply online through the Institute’s website. Applications submitted through any other mode will not be accepted.
Follow the step-wise procedure:
- Step 1: Details of applicant – Provide your personal and contact details accurately.
- Step 2: Uploading of documents – Upload all the required documents in the specified formats.
- Step 3: Payment of application fee – Make the non-refundable application fee payment using Debit Card / Credit Card / Internet Banking / UPI. Please note that no correction or modification is possible once payment is made, and the fee will not be refunded.
Upon successful submission, an auto-generated email containing the reference number will be sent to your registered email address. Keep this reference number for all future correspondence.
Candidates are advised to keep a printout of the online application form for their records.
It is crucial for candidates to ensure they fulfil all the eligibility criteria as stipulated in this advertisement. Failure to meet the criteria at any stage will lead to cancellation of candidature/termination.
Incomplete applications will be summarily rejected, and no correspondence will be entertained regarding them.
In case of any difficulty during the online application process, please send an e-mail to HR.CDSA@THSTI.RES.IN, attaching a screenshot of the error displayed.

Important Links

Quick Access
Direct Online Application Link	Apply Now
Official Notification	Click Here
Official THSTI Website	Visit Website

“Government strives to have a work force which reflects gender balance and women candidates are encouraged to apply”

(M.V. Santo)
Head-Administration

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BRIC-THSTI CDSA Recruitment 2025: Project Research Scientist (B.Pharm/Pharm.D/Medical) Jobs

RECRUITMENT NOTIFICATION: PROJECT POSITIONS AT CDSA CENTER

About THSTI and CDSA

Recruitment Summary

Available Vacancies

Educational Qualifications & Experience

Job Profile and Responsibilities

Required Skills

Application Fee Details

General Terms & Conditions

How to Apply Online

Documents to Keep Handy Before Filling the Online Application (PDF format for all except photo/signature):

Step-wise Online Application Process:

Important Links

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One thought on “BRIC-THSTI CDSA Recruitment 2025: Project Research Scientist (B.Pharm/Pharm.D/Medical) Jobs”