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1

clinical research coordinator

  • Ongoing clinical trial coordination from start-up to close-out
  • Worked within small teams of a broad organisation, requiring excellent and efficient communication skills across departments
  • Liaised with clinical research associates, sponsor representatives, medical staff and study participants
  • Conduct of studies in accordance with ICH-GCP guidelines 
  • Development and management of source documentation and databases; ongoing data entry
  • Performed assessments e.g. vital signs and ECG measurement, venepuncture, spirometry, collection of demographic information
  • Blood and urine sample processing  
2

clinical research coordinator

  • Coordinating clinical research in a collaborative and interdisciplinary environment using intracranial EEG (iEEG) with epilepsy patients and MRI/fMRI with patients and healthy controls 
  • Led participant involvement: eligibility determination, recruitment, consenting, running behavioural tasks
  • Maintaining daily communication with lead investigator, research collaborators and clinical team
  • Technical supervision and assistance, data acquisition, database management, data storage
  • Grant submissions, maintaining ethics documents (protocols, consent forms)
  • Hiring, training, and supervising volunteers, project development and planning, mentoring
  • Maintaining lab websites, organizing meetings, and ordering lab equipment
3

clinical research coordinator

  • Take part in preparation and control of research budgets and financial payments.
  • Notify subjects regarding all study aspects relevant to them.
  • Enter study data into the applicable database.
  • Manage necessary records of study related activity which includes case report forms, drug dispensation records etc.
  • Communicate with laboratories or researchers about laboratory findings.
  • Take part in meetings and seminars to update knowledge of clinical research and related issues.
  • Enrol subjects in the study as per the study protocol.
4

clinical research coordinator

  • Screening and recruitment of study subjects 
  • Maintenance of research databases
  • Provide support for research studies including IRB submissions, answering IRB queries, 
  • Obtaining informed consent collecting study samples, scheduling patient visits, processing biological specimens
  • Maintain study site files
  • Randomization as part of unblinded team
5

clinical research coordinator

  • Worked as researcher in-vitro fertility drugs, to work with the study based on protocol, explain a consent form to subject, maintains subjects case reports form (CRF)
  • Trained and supervised junior staff in various SOPs and study-specific tasks
  • Prepare or get involved in quality assurance audits performed by study sponsors, regulatory authorities, or exclusively designated review groups.
  • Prepare advertising and other educational materials and conduct campaigns to enroll subjects.