Research Coordinator

Job summary: The Research Coordinator will support the planning, implementation, and management of research projects. They will ensure studies are conducted according to protocol, standard operating procedures (SOPs), good clinical practice (GCP), and applicable regulations. The coordinator will also be responsible for maintaining accurate records, organizing and updating study files, and ensuring proper documentation and data integrity in accordance with institutional and regulatory requirements.

Key Responsibilities:

Coordinate day-to-day activities of assigned research studies. Assist with protocol development and study documentation. Maintain accurate and complete records. Manage data collection, entry, cleaning, and preliminary analysis. Communicate effectively with investigators, research team members, sponsors, and collaborators. Ensure regulatory compliance and proper reporting of adverse events. Organize research meetings, trainings, and visits. Assist in preparing reports, abstracts, presentations, and publications. Maintain confidentiality and data security at all times. Contribute to quality improvement initiatives within the research program.

Requirements

MPH or Bachelor's degree in Life Sciences, M.Sc. in Clinical Research, or PG Diploma in Clinical Research/Health Sciences Prior

experience

(0 - 1 years) coordinating clinical or field research preferred. Knowledge of research ethics, GCP, and regulatory guidelines. Excellent organizational, communication, and interpersonal skills. Proficiency in MS Office Suite (Word, Excel, PowerPoint) Ability to manage multiple tasks, set priorities, and work independently with minimal supervision.

Key Responsibilities:

Coordinate day-to-day activities of assigned research studies. Assist with protocol development and study documentation. Maintain accurate and complete records. Manage data collection, entry, cleaning, and preliminary analysis. Communicate effectively with investigators, research team members, sponsors, and collaborators. Ensure regulatory compliance and proper reporting of adverse events. Organize research meetings, trainings, and visits. Assist in preparing reports, abstracts, presentations, and publications. Maintain confidentiality and data security at all times. Contribute to quality improvement initiatives within the research program.

Requirements

MPH or Bachelor's degree in Life Sciences, M.Sc. in Clinical Research, or PG Diploma in Clinical Research/Health Sciences Prior

experience

(0 - 1 years) coordinating clinical or field research preferred. Knowledge of research ethics, GCP, and regulatory guidelines. Excellent organizational, communication, and interpersonal skills. Proficiency in MS Office Suite (Word, Excel, PowerPoint) Ability to manage multiple tasks, set priorities, and work independently with minimal supervision.