Facilitate the review and negotiation of clinical trial agreements (CTAs) and investigator grants between PSI Legal, the project team, and the study site.
Customize and prepare contractually binding site-specific documents in cooperation with PSI Legal.
Facilitating negotiations of site agreements and budgets to ensure alignment with the site activation plan.
Customizing and preparing country- and site-specific agreements and organizing their translations.
Tracking the status of site agreement and budget negotiation.
They are a company that cares for their staff, clients, partners and the quality of their work. A dynamic, global company founded in 1995, they bring together more than 3000 driven, dedicated and passionate individuals, working on the front line of medical science, changing lives, and bringing new medicines to those who need them.
Serve as the subject matter expert and primary escalation point for global site contracts, budgets, and payments
Lead development of investigator grant budgets, payment terms, and contracting strategies
Oversee contract tracking, documentation, and compliance across internal systems and external partners
Deciphera is committed to equal employment opportunity and values diversity. They provide a competitive compensation and benefits package to all employees and believe in personal and professional growth.
Assist with investigator recruitment activities and site feasibility tasks.
Perform essential document collection, review, and maintenance activities.
Act as site contact for study and site management issues.
Precision for Medicine supports life sciences companies in the use of precision medicine by helping them design and execute clinical trials. They focus on biomarker-led strategies and have expertise in data science, clinical trial management, and laboratory services.
Prepare budgets, proposal text and re-bids to support RFP responses.
Coordinate RFP development meetings with sales, operational review and finance teams.
Ensure accuracy and quality control of budget and proposal text edits.
Precision for Medicine is a precision medicine CRO with a uniquely integrated offering. They combine novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.
Conduct and report all types of onsite monitoring visits as well as remote visits.
Perform CRF review, source document verification and query resolution.
Be responsible for site communication and management.
PSI is a dynamic, global, mid-size company founded in 1995, bringing together more than 3,000 driven, dedicated, and passionate individuals. They work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
Oversees and supports country level feasibility, Investigator identification and selection, if applicable.
Responsible for overall management of project allocated direct reports (CRAs, Site Managers and CTAs, as applicable).
Coordinates and ensures the adequate preparations for site specific audits and inspections.
Ergomed is a rapidly expanding full-service mid-sized CRO specializing in Oncology and Rare Disease. They have operations in Europe, North America and Asia and values employee experience, well-being and mental health.