Clinical Research

2 weeks ago


Remote, India IPR LEARNING INSTITUTE Full time

**Responsibilities**:

- Assist in the planning, execution, and monitoring of clinical research studies.
- Ensure compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Monitor and report adverse drug reactions (ADRs) and other pharmacovigilance activities.
- Conduct literature reviews and safety signal assessments.
- Maintain accurate records and documentation related to clinical trials and pharmacovigilance activities.
- Collaborate with cross-functional teams including regulatory affairs, quality assurance, and medical affairs.
- Support in drafting and reviewing safety reports and regulatory submissions.
- Ensure timely reporting of safety data to health authorities and stakeholders.

**Qualifications & Skills**:

- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, or a related field.
- 1-3 years of experience in clinical research, pharmacovigilance, or a related area (freshers with relevant knowledge may also apply).
- Knowledge of ICH-GCP guidelines, regulatory requirements, and pharmacovigilance principles.
- Strong analytical and problem-solving skills.
- Excellent communication and teamwork abilities.
- Attention to detail and ability to handle data with accuracy.
- Proficiency in Microsoft Office (Word, Excel, PowerPoint).

**Job Types**: Full-time, Fresher, Internship

Pay: From ₹300,000.00 per year

Schedule:

- Day shift
- Morning shift

Work Location: Remote


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