Clinical Research Associate
Allucent · Bengaluru · onsite · Posted 29d ago
Undisclosed5–10 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
Job Summary
Responsibilities
Requirements
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
As a CRA , you will take the lead on monitoring activities, owning your sites and relationships with investigators. You ll be the bridge between sponsor and site, ensuring trial integrity while being supported by a collaborative, experienced team. This includes work related to regulatory affairs, site activation processes-including contracting and start-up activities-to ensure smooth and compliant study execution.
Responsibilities
- Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits.
- Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements.
- Build strong site relationships, acting as a primary point of contact and ensuring high-quality data collection.
- Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety.
- Activities around regulatory affairs, site activation and study-startup.
Requirements
- Haemophilia trial experience is must along with monitoring experience Haemophilia study .
- You re an experienced CRA ready to take the next step with a company that truly values your expertise and independence. You thrive in an agile, collaborative environment and want to be part of a team making a real impact.
- Experience leading monitoring activities in complex trials, ideally in oncology or rare disease with a minimum of at least 5 years experience.
- Strong understanding of ICH-GCP and regulatory guidelines .
- Comfortable working independently and managing priorities.
- Willingness to travel, as required.
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
Sourced from naukri
Skills
Agilepharmaceuticalsemployee referralclinical researchclinical trialshuman resourcesgoogle cloud platformRegulatory Affairspatient safetyTalent AcquisitionSite InitiationoncologyResearchData Collectionoperationscompliance
About Allucent
Allucent
Pharma
Chennai, Tamil Nadu
India
₹15.4L PA avg
Avg at Allucent
About
Allucent specializes in overcoming unique challenges faced by small and mid-sized biotech firms, offering global drug development services across diverse therapeutic areas.
Industries
BiotechnologyPharmaceutical
Employee ratings
10 reviews
3.2/ 5
Culture
2.5
Career growth
2.8
Work-life
2.9
Employees rate it well for
Company Culture32Compensation & Benefits32
Find them on