Dear Students,
Greetings from CLRI!!
Great opportunity to gain hands-on experience in a CRC role.
Students who have taken ADCR/ PG Diploma in Clinical Research are eligible to apply.
It gives us immense pleasure to announce that SunSecure Clinical Research Services Pvt Ltd has shown interest in hiring talent from Clinilaunch Research Institute.
About the Company
Sunsecure Clinical Research Services Pvt Ltd, headquartered in Bangalore, extends a competitive edge to its clients. Our operational base in Bangalore empowers us to deliver unmatched advantages to our esteemed clientele. Our service model spans a diverse array of domains, ensuring that we cater to a comprehensive spectrum of needs within the clinical research arena.
Our multifaceted service offerings encompass site management, clinical monitoring, clinical audits, regulatory support, clinical staffing, protocol writing, clinical data management, pharmacovigilance, and a range of allied services. This extensive array of services is meticulously designed to cater to the unique requirements of our clientele.
Website: https://www.sunsecure.co.in/about
Job Type: Private
Hiring For: SunSecure Clinical Research
Job Role : Clinical research coordinator
Industry: Clinical research services
Job Priority: Normal
Job Nature: Office
Job Mode: Full Time
Job Position: Permanent
Job Location: Bangalore
Salary Range: First 3 months training (Unpaid)
After that 15,000 per month.
Experience Range: Freshers (Only Females)
Qualification: B.Pharma (Localites)
Interview mod: telephonic and Walk in
Date Published : 27-1-2026
Valid Through : 27-1-2026 ( 12: 30 PM )
Languages: Mandatory Kannada
Key Responsibilities
*Recruit and enrol participants as per Investigator’s instructions/recommendations.
*Assess the eligibility of potential participants through interviews, medical records reviews,
and discussions with physicians and nurses.
*Ensure protocol and SOP compliance
* Ensure that the study adheres to regulations, Good Clinical Practice (GCP) standards, and
*Institutional Ethics Committee (IEC) requirements.
* Collect and review data, and prepare study-related documentation.
*Make data entries (electronic or paper), obtain review/signatures from the investigators on all the source documents.
*Manage participants . Serve as a primary point of contact for study participants, ensuring their safety and wellbeing.
* Collaborate with the research team – CRO/Sponsor team to address issues that arise and ensure the study runs smoothly.
* Assist the Investigators in notifying the Ethics Committee/Sponsor/CDSCO on Adverse Events/ Serious Adverse Events.
*Assist the Investigators in notifying the Ethics Committee/Sponsor on Protocol Deviations.
*Ensure the accountability of all the trial related logistics, both IP and non-IP related inventories.
* Assist the clinical trial monitors/ sponsor representatives during their site visits, viz., site selection visits, initiation visits, monitoring visits, booster visits, close out visits etc.
*Any other activity as designated by the Line manager / Investigator.
Application link: https://forms.gle/fRL5FUnkpQxZpEq99
For any queries, contact:
Name : Kala N G, Priyanka C, and Pooja Nayak
Contact No : 7204412729, 8904527576, & 9606048331
Regards,
CliniLaunch - Placement team.