Responsible for site monitoring activities including interim monitoring visits to clinical sites, site initiation, and close-out visits
Responsible for site management activities
General On-Site Monitoring Responsibilities
Ensure the study staff who will conduct the protocol have received proper training and delegation
Ensure the protection of study patients
Ensure accuracy of the data submitted
Monitor data for missing or incorrect data
Travel up to 80% is required
Prepare accurate and timely trip reports
Complete Serious Adverse Event (SAE) reporting and follow up of SAEs
Independently perform CRF review
Perform other duties as assigned by management
University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing license),
a minimum of 2 years of clinical research experience, 5 years preferred.
Hematology/oncology experience required. Bone marrow transplant and/or immune cell therapy experience is preferred.
Telecommuting is allowed.
Additional Salary Information: All employee benefits paid. Three weeks paid vacation.
Internal Number: BellicumCra3
About Tranquil Clinical and Research
At Tranquil Clinical and Research Consulting Services, our ultimate goal is excellence in the clinical trial process and bringing trustworthy products to patients.Tranquil Clinical Research was created to ensure that the entire clinical trial, device, and drug development process is conducted with ethics and the patient in mind first and always. Our business model ensures a client’s drug, device or investigatory product in the clinical trial is adherent to the highest level of quality and integrity in the services we provide.We have 8 employees, a business attorney, a business advisor, accountant and book keeper. We are based in Friendswood, TX, however our employees are regional throughout the US.