• Implemented and monitored clinical trials to ensure sponsor and investigator obligations were being met and are compliant with applicable local regulatory requirements and ICH guidelines.• Visited sites to assess the qualification of potential investigative sites, initiate studies, instructed site personnel on the proper conduct of studies, to review data and ensure accuracy of data collected and to terminate studies.• Provided regular clinical status information to team members and project management.• Performed billable work in accordance with SIII policies, procedures, and Standard Operating Procedures (SOPs)Worked closely with other team members to ensure timely resolution of projects.• Communicated common site trends to Lead CRA/Clinical Trial Manager and other project team members.• Visited including Site Selection Visit, Initiation Visit, Interim Monitoring Visit, and Close Out Visits• Performed investigative site file reconciliation; requested any new or updated site-related essential and non-essential documents and reviews them for content, consistency with other documents, and compliance with appropriate local regulatory requirements, ICH guidelines, project SOPs, and sponsor requirements.• Performed source document verification and performed query resolution in a timely manner and oversees drug accountability and safety at investigative sites.• Ensured Serious Adverse Event (SAE) reporting per project specifications.• Responded to requests from investigative sites in a timely fashion.

Managed and led all aspects of laboratory functions focused on facilitated research into genetic causes of disease. Conducted complex research, gathered information from multiple sources, and delivered reports on results.• Carried out quality control assessments for DNA analysis software and ensured all research activities adhered to time schedules.• Excellent computer skills.• Excellent organizational skills.• Knowledge of medical terminology.• knowledge of GCP.

Partnered with physicians to assist with various procedures including stiches, wound packing, IV placement, and organizing/maintaining all necessary supplies and equipment, while participating in the delivery of patient care excellence in accordance to care plans and physician instructions.• Worked alongside experienced nursing professionals to learn new procedures and managed/observed patients recovering from medical or surgical procedures.• Collaborated with nurse preceptors and other medical staff to achieve quality patient outcome goals and built trusting rapport with patients and members of each patient’s support system.• Updated patient charts and documented all medication administration to ensure records remained current and supported treatment regimes.• Assisted patients with personal hygiene and monitored temperature, pulse, respiration, blood pressure, and patient status to detect/report any deviations or issues to the supervising nurse or administrator.• Recording details and symptoms of patient medical history and current health.• Preparing patients for exams and treatment.• Creating, implementing, and evaluating patient care plans with the medical team.• Performing wound care, such as cleaning and bandaging them.• Operating and monitoring medical equipment.• Drawing blood, urine samples, and other body fluids for lab work.• Educating patients and family members on treatment and care plans, as well as answering their questions.