Position Type: [Full-Time/Part-Time/Contract]

Position Summary:
We are seeking a highly organized and motivated Research Coordinator to oversee and support research projects. The Research Coordinator will be responsible for managing day-to-day research activities, ensuring compliance with regulatory standards, and facilitating communication between investigators, participants, and stakeholders.

Key Responsibilities:

• Coordinate and manage the daily operations of research studies.

• Assist in the development of study documents, consent forms, and ethics submissions.

• Recruit and screen study participants; schedule and conduct study visits.

• Maintain detailed and accurate study records and databases.

• Monitor study progress to ensure adherence to timelines and protocols.

• Communicate effectively with research team members, collaborators, and regulatory bodies.

• Prepare progress reports, publications, and presentations as needed.

Qualifications:

• Bachelor's degree in health sciences, life sciences, public health, or a related field preferred.

• Previous experience in psychiatry, neurology and oncology as a clinical trial coordination is strongly preferred.

• Familiarity with ethical and regulatory guidelines (e.g., IRB, GCP).

• Strong organizational, communication, and problem-solving skills.

• Proficiency in Microsoft Office and research software/databases (e.g., REDCap, SPSS) is an asset.

Application Process:
Interested candidates should submit a resume to
[email protected]