Clinical Research Coordinator

11 hours ago

Kharadi Pune Maharashtra, India Pacifix Research Full time

Pacifix Research is seeking a motivated and detail-oriented Clinical Research Coordinator to join our team. This is an excellent opportunity for fresh graduates interested in starting their career in clinical research. The Clinical Research Coordinator will play a crucial role in coordinating and managing clinical trials, ensuring compliance with regulatory requirements, and maintaining the highest standards of clinical research.

**Key Responsibilities**:

- **Study Coordination**: Assist in the planning, implementation, and management of clinical research studies. Coordinate with study teams to ensure all aspects of the trial are conducted according to the study protocol.
- **Participant Recruitment**: Identify, recruit, and screen potential study participants according to the study protocol and inclusion/exclusion criteria.
- **Data Collection**: Collect, record, and maintain accurate study data and patient information. Ensure data integrity and compliance with regulatory standards.
- **Regulatory Compliance**: Ensure that all study activities are conducted in compliance with ethical standards, Good Clinical Practice (GCP) guidelines, and applicable regulations.
- **Documentation**: Maintain and update study documents, including case report forms, consent forms, and study logs. Assist in preparing study reports and submissions to regulatory bodies.
- **Patient Communication**: Serve as a point of contact for study participants, providing them with information about the study, addressing concerns, and ensuring informed consent is obtained.
- **Quality Assurance**: Monitor study progress and ensure that all procedures are performed according to protocol. Assist in identifying and resolving issues related to study conduct.
- **Collaboration**: Work closely with investigators, study sponsors, and other team members to ensure smooth study operations.

**Required Skills**:

- **Educational Background**: Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related field. Fresh graduates are welcome to apply.
- **Attention to Detail**: Strong attention to detail and accuracy in data collection and documentation.
- **Communication Skills**: Excellent verbal and written communication skills. Ability to interact effectively with study participants, healthcare professionals, and team members.
- **Organizational Skills**: Strong organizational and time management skills, with the ability to manage multiple tasks and prioritize effectively.
- **Problem-Solving**: Ability to identify problems and propose solutions to ensure the smooth conduct of clinical trials.
- **Technical Proficiency**: Basic knowledge of Microsoft Office (Word, Excel, PowerPoint). Familiarity with clinical research software is a plus.
- **Ethical Standards**: Understanding of ethical principles in clinical research and commitment to maintaining patient confidentiality.

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

**Education**:

- Bachelor's (preferred)

**Experience**:

- total work: 1 year (preferred)

Work Location: In person

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