Overseeing research projects from start to finish, including design, data collection, and analysis. They may also manage day-to-day operations, such as budgets, timelines, and reporting requirements.CollaboratingWorking with other researchers, scholars, and stakeholders to design experiments, compare results, and ensure projects meet scientific and ethical standards.Finding fundingIdentifying potential sponsors and funding opportunities, and writing proposals for new or renewed research.Interpreting findingsCommunicating research results to a variety of audiences, such as Congress, the public, and the criminal justice community. This can include presenting findings in reports, policy briefs, white papers, conferences, and peer-reviewed publications.

Responsible for coordinating and managing CRA activities. • Oversaw appropriate planning and tracking of monitoring visits. • Reviewed site visit reports. • Development of site management related documents (manuals, templates, and tools). • Providing CRA specific guidance, training, and coaching. • Oversaw and managed site communications and site issues until resolution. • Oversaw centralized and risk-based monitoring activities. • Managed study progress relative to enrollment and monitoring.

Built relationships. Oversaw integrity of the study and utilize problem-solving skills to promote rapport with the site and staff. Protected patients. Reviewed the performance of the trial at designated sites, ensured the rights and well-being of human subjects are safeguarded and are in accordance with protocol. Developed patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while also ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s).

Assisted in participant recruitment and retention activities and assisted in screening potential study participants for eligibility. Performed study procedures, routine tests, data collection/recording, and daily operations of moderate risk clinical research protocols. Collected, processed, packed, and shipped specimens according to protocol, applicable standards and regulations. Maintained study binders and filings according to protocol requirements and department policy.

Educated patients and families on medical-surgical procedures, therapeutic regimens and pain management techniques. Admission, teaching and discharge of patients, routine drug administration, IV including Blood transfusion, IM, sub-acute and oral drug administration. Pre-operative nursing care and post-operative care to patients who had surgeries and minor procedures Admission and discharge, routine drug administration, accident and emergency care Admission and discharge, routine drug administration, accident and emergency care Taking patient blood samples, pulses, temperatures and blood pressures. Experience of chronic disease management i.e. diabetes and asthma