Clinical Research Coordinator

Job Description:

Are you passionate about contributing to the advancement of medical science and improving healthcare outcomes? Do you possess strong organizational skills and attention to detail? If so, we have an exciting opportunity for you to join our team as a Clinical Research Coordinator.

About Us:

We are a leading healthcare organization dedicated to conducting groundbreaking research and clinical trials to enhance the understanding and treatment of various medical conditions. Our commitment to excellence and innovation drives us to collaborate with top medical professionals and institutions worldwide.

Key Responsibilities:

As a Clinical Research Coordinator, you will play a pivotal role in the execution and coordination of clinical research studies. Your responsibilities will include, but are not limited to:

1. Protocol Management: Facilitate the implementation of research protocols by ensuring adherence to regulatory guidelines and study procedures.
2. Participant Recruitment: Collaborate with healthcare providers to identify and enroll eligible participants for clinical trials. Engage in outreach efforts to inform the community about research opportunities.
3. Informed Consent Process: Guide participants through the informed consent process, ensuring comprehension and ethical considerations are addressed.
4. Data Collection and Management: Oversee the collection, recording, and management of study data in compliance with regulatory standards and study protocols.
5. Coordination with Investigators: Serve as a liaison between principal investigators, study sponsors, and research staff to ensure seamless communication and execution of study activities.
6. Participant Monitoring: Conduct regular follow-up assessments with participants to monitor their progress and ensure compliance with study requirements.
7. Adverse Event Reporting: Promptly report any adverse events or deviations from the protocol to the appropriate regulatory bodies and study sponsors.
8. Quality Assurance: Implement quality control measures to maintain the integrity and accuracy of study data. Participate in internal and external audits as required.
9. Documentation and Reporting: Prepare comprehensive study documentation, including study protocols, case report forms, and study reports. Generate timely progress reports for study sponsors and regulatory authorities.
10. Continuing Education: Stay updated on relevant regulations, guidelines, and best practices in clinical research. Participate in training sessions and professional development activities to enhance knowledge and skills.

Qualifications:

To excel in this role, you should possess the following qualifications:

• Education: Bachelor's degree in life sciences, nursing, pharmacy, or a related field. Advanced degrees or certifications in clinical research are preferred but not required.
• Experience: While prior experience in clinical research is advantageous, we welcome applications from motivated individuals, including fresh graduates, who demonstrate a strong interest in the field.
• Skills: Excellent communication, interpersonal, and organizational skills are essential. Proficiency in Microsoft Office suite and electronic data capture systems is desirable.
• Ethical Standards: Uphold the highest ethical standards in all aspects of research conduct, ensuring participant safety, privacy, and confidentiality.
• Team Player: Collaborate effectively with multidisciplinary teams, including physicians, scientists, and research coordinators, to achieve common goals.

Apply Now:

If you are ready to embark on an exciting journey in clinical research and contribute to meaningful advancements in healthcare, we encourage you to apply now by clicking on the "Apply For Job" button below. Join us in making a difference in the lives of patients and communities worldwide.