Strong knowledge of the clinical research process, including working knowledge of all functional areas of clinical trials and medical terminology. Experience in oncology or infectious disease required
Experience in monitoring and/or coordinating clinical trials or collection studies required. But this profile does not require on-site monitoring/visits as most of the work is handled virtually
Excellent written and verbal communication skills is MUST to express complex ideas to study personnel at research and clinical institutions
Demonstrated ability to form strong functional relationships
Excellent presentation, organizational and interpersonal skills. Ability to interact with all levels of staff to coordinate/execute study activities
Ability to handle several priorities within multiple, complex research
Ability to reason independently and recommend specific solutions in clinical settings
Ability to work independently, prioritize, and work within a matrix team environment
Ability to mentor other CRAs and co-monitor, as required
Knowledge of current GCP/ICH guidelines applicable to the conduct of clinical research