Clinical Research

2 weeks ago


Kolkata, India Infoclin Consultancy Full time

**Payroll**- Direct

**Knowledge part**:
Thorough knowledge of ICH - GCP, New Drugs and Clinical Trials rule 2019
and updating self from time to time on Regulatory and process changes (if any).
Action part:
P.I. Coordination, Patients screening, randomization, source documentation,
site master file maintenance, eCRF entry, PK/ ADA sample collection, storage,
lab report collection, reporting & follow up SAEs, Ethics committee
coordination, study doc archiving.
Excellent verbal & written communication skills.
High Potential, enthusiastic, accountable
Positive Work ethic & good attitude
Team Player
Presentation Skills
Excellent Leader
Interpersonal & motivational skills

**Industry Type**: Pharma/ Biotech/Clinical Research

**Experience**:
0.6 - 1 year

**Salary**:
Discuss over interview.

**Education**:
B.Pharm, B.Sc, M.Pharm, M.Sc,

**Location**:
All over India



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