Posted:2 hours ago|
Platform:
On-site
Full Time
Assist in site selection, initiation, monitoring, and close-out visits under supervision.
Ensure that clinical trials are conducted in accordance with ICH-GCP guidelines, SOPs, and regulatory requirements.
Verify accuracy, completeness, and consistency of Case Report Forms (CRFs) and other study documentation.
Support in maintaining essential clinical trial documents and trial master files.
Collaborate with investigators, site staff, and project teams to ensure smooth trial operations.
Assist in reporting adverse events and ensuring patient safety compliance.
Participate in training programs and workshops to build technical knowledge and monitoring skills.
CLARIWELLGLOBAL SERVICES LLP
Upload Resume
Drag or click to upload
Your data is secure with us, protected by advanced encryption.
Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.
We have sent an OTP to your contact. Please enter it below to verify.
Instantly access job listings, apply easily, and track applications.
Experience: Not specified
7e-05 - 0.00011 Lacs P.A.
0.5 - 0.6 Lacs P.A.
bengaluru, karnataka, india
Experience: Not specified
Salary: Not disclosed
pune, maharashtra, india
Experience: Not specified
2.5 - 3.0 Lacs P.A.
bengaluru, karnataka, india
Salary: Not disclosed
chennai, tamil nadu
Salary: Not disclosed
0.5 - 0.6 Lacs P.A.
bengaluru
Experience: Not specified
1.0 - 5.0 Lacs P.A.
bengaluru, karnataka
Experience: Not specified
1.0 - 5.0 Lacs P.A.
2.5 - 5.5 Lacs P.A.
