Clinical Trial Associate

Details of the offer

Company Overview Tango Therapeutics is a biotechnologycompanydedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer.
Using an approach that starts and ends with patients, Tango leverages the genetic principle of synthetic lethality to discover and develop therapies that take aim at critical targets in cancer.
This includes expanding the universe of precision oncology targets into novel areas such as tumor suppressor gene loss and their contribution to the ability of cancer cells to evade immune cell killing.
The Tango labs and offices are located at201 Brookline Avenue, in the Fenway area of Boston, Massachusetts
Summary In this exciting new role, you will provide clinical trial coordination support to the assigned clinical trial or trials. This support includes study deliverable tracking and completion of study documentation including eTMF is maintained for the assigned clinical trial(s). You will work with internal clinical team members and with external vendors and CROs. The position reports to the Clinical Operations Program Lead. May work collaboratively on one program or across several trials to support clinical operations activities.
Your Role: You will coordinate support from start up to close out for assigned trialsOngoing eTMF maintenance and completion with CRO for assigned trialsMeeting coordination and documentationTracking of action items for clinical deliverablesReconciliation and tracking of purchase orders and invoices for assigned trialsDaily study management for assigned clinical trial(s) or assigned region in larger studiesOwnership of clinical trial tracking documentsMay include clinical sample tracking and coordinationEnsure trial management documentation is conducted in accordance with ICH/GCP standardsDevelop and maintain strong, collaborative relationships with multiple cross functional team membersAdditional duties and responsibilities as requiredWhat You Bring: At least 2 years of trial coordination experience in a clinical research environment, with at least some within the biotech/pharma industryBachelor's Degree in a life-science-based subjectOncology therapeutic experience preferredBasic understanding of drug developmentUnderstanding of FDA and ICH GCP guidelines to ensure the appropriate conduct of clinical studiesGood verbal and written communication skillsGood organizational skills and attention to detailWe are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. #LI-Hybrid

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Nominal Salary: To be agreed

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