0 - 2 years
0 Lacs
Posted:5 days ago|
Platform:
On-site
Full Time
Assist in preparing essential trial documents (Investigator Site File, Trial Master File, etc.).
Support site selection, initiation, monitoring, and close-out activities.
Ensure accuracy and completeness of study documents.
Support senior CRAs during routine monitoring visits.
Verify source documents, patient eligibility, and informed consent forms.
Ensure adherence to study protocols and GCP norms.
Assist in data collection, query resolution, and CRF/EDC data entry checks.
Ensure timely reporting of deviations and adverse events.
Ensure that all trial activities follow SOPs, regulatory guidelines, ICH-GCP, and ethical standards.
Maintain confidentiality and integrity of clinical trial data.
Coordinate between investigators, study coordinators, and project teams.
Attend training sessions, investigator meetings, and team discussions.
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.
bangalore, hyderabad, pune, mumbai city, delhi
Experience: Not specified
7e-05 - 0.00012 Lacs P.A.
mumbai, maharashtra, india
Experience: Not specified
Salary: Not disclosed
hyderabad, all india
Salary: Not disclosed
bangalore, iran, guinea, faridkot, coimbatore, zimbabwe, iraq, chennai, raipur, hyderabad, kolkata, lebanon, faridabad, guinea bissau, zambia, mumbai city, chandigarh, kenya, equatorial guinea
0.00016 - 0.00022 Lacs P.A.
4.25 - 8.0 Lacs P.A.
bhubaneswar, all india
Salary: Not disclosed
ahmedabad
Experience: Not specified
2.90604 - 5.25372 Lacs P.A.
delhi, delhi, india
Salary: Not disclosed
prabhadevi, mumbai, maharashtra
1.8 - 2.4 Lacs P.A.
prabhadevi, mumbai, maharashtra
Experience: Not specified
0.15 - 0.2 Lacs P.A.