Qualifications Actual Job Title: Global Trial Optimization Associate Education: Bachelor s or higher degree should be in-progress with a focus in a medical, pharmaceutical, public health, or biology field of study. Core Skills Knowledge of GCP and clinical research development Ability to manage multiple competing priorities with good time management and prioritization skills Strong interpersonal skills Strong communication, writing and presentation skills Intermediate knowledge of Microsoft office or similar (Excel, PowerPoint, Word, Outlook, etc.) Required Skills: Knowledge of GCP and clinical research development Ability to manage multiple competing priorities with good time management and prioritization skills Strong interpersonal skills Strong communication, writing and presentation skills Intermediate knowledge of Microsoft office or similar (Excel, PowerPoint, Word, Outlook, etc.) Preferred Skills: Prior experience in clinical operations/clinical research with the conduct of clinical trials is preferred Competency in medical data terminology; data analysis Strong administrative and project management skills in a relevant clinical development setting. Strong interpersonal and communication skills Eagerness to learn and the ability to work across multiple activities simultaneously Note: 100% remote role. Part time role Should be able to work any time between 8am-5pm EST.
Responsibilities Our Clinical Research teams push the boundaries of global healthcare through research and innovation. Under the supervision of the Indication Lead Global Trial Optimization Specialist, this position will be responsible to create deliverables for operational planning that will be used for projecting study timelines, conducting site feasibility, estimating operational parameters, and facilitating country selection and recruitment and retention efforts in support of our company s clinical trials. This position is part of our mission to provide opportunities in support of our function s early talent development program. Job Responsibilities Under the mentorship of the Indication Lead Global Trial Optimization Specialist, will create functional area deliverables that support clinical study planning and recruitment. These may include but are not limited to: Creation of patient and site facing recruitment materials Creation of the site feasibility questionnaire Creation of trial and program level slide decks Project management of recruitment vendors Database searches and data analysis Dependent on experience, may serve as the Global Trial Optimization Specialist on the clinical trial team Contributes to functional area process improvement and training initiatives
Comments/Special InstructionsSr. CSP Vidushi Sharma. This is a part time role. Submit your best 2 qualified candidates. This is not a site selection CRA position.
System Location:, Research Labs (Z011), Required
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CWR Type:, W-2, Required