Global Sr CTM - Home Based in SPAIN. FSP. Vendor experience required

Syneos Health, Inc.; España; Remote; EUR 90.000 - 120.000; Vollzeit

Zusammenfassung

Syneos Health, Inc. is seeking a Global Sr CTM to operate remotely from Spain. The role involves managing global/multi-country studies and various vendor types to ensure timely delivery and quality across sponsor projects.

The candidate should bring strong CTM leadership, budget oversight, and cross-country coordination capabilities to drive study timelines and process improvements in a fast-paced environment.

Qualifikationen

• Experience as CTM in the management of global/multiple-country studies and different types of vendors is required.

Aufgaben

• Develop protocol concepts and review Clinical Study Protocols and amendments.
• Manage budgets, CDAs, and vendor invoices; support overall study budgeting.
• Assist with country/site feasibility, site selection, and Feasibility Questionnaires; Green Light Letters.

Kenntnisse

CTM experience

Jobbeschreibung

Global Sr CTM - Home Based in SPAIN. FSP. Vendor experience required

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver - for one another, our customers, and, most importantly, for those in need.

Discover what your 25,000 future colleagues already know:

Why Syneos Health

• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
• We are committed to building an inclusive culture - where you can authentically be yourself. Central to this is our purpose - Driven to Deliver - which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone's life.
• We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

Job Responsibilities

Experience as CTM in the management of global/multiple-countries studies and different types of vendors is required

Main tasks

• Protocol Development : Support the development and review of the Clinical Study Blueprint (CSB) and Protocol, and all Amendments and/or Administrative Changes
• Budget : Manage the execution of the CDAs; support Project Managers in the creation of overall study budget (working with the contract/budget analyst); support site contract amendments and negotiation; manage invoices
• Country and Site Feasibility and Selection : assist in development of Investigator Site Selection Plan; attend country and site selection Jams; Assist with creation of Feasibility Questionnaire; assist with Site Selection and Green Light Letters, if applicable
• Site/Country Contracts and Budgets : stay informed of progress with CDAs, CSA and site budgets; support sites for contract amendments; assist with negotiation for site contracts
• Financial/Payment Management : oversight of site payments and vendor payments, if applicable
• Study Budget Financial Reconciliation : draft and facilitate the Clinical Study Budget review
• Clinical Study Timelines : Support the planning for the clinical study timelines, finalization and update of clinical study timelines; and manage the study team to meet all timelines
• Study Team Training : Assist/support in the creation/finalization of Study Specific Training (TA training, Compound, Study Design, Vendors, Eligibility, etc); Facilitate training sessions; Assign training as appropriate; assist with creation/finalization of Study Monitor Training materials
• Site Training : Assist Project manager in planning for the Investigator Meeting; creation of and collection of slides from all functional areas to create the final master deck for the IM; presenting at the IM, filing documentation of training
• Data Management and Closeout : Review updates to Data Managemet Plan; Interim/Final Db Lock Preparation (drive study DBL completeness); Interim/Final Database Lock Preparation (Responsible for study DBL completeness)
• Plans : Site Selection Plan, Study-Specific Issue Management Plan , Vendor Oversight Plan, TMF Artifact Map and Plan
• Clinical Supplies : Assess and review of materials by external vendors (lab kits, ePRO devices, eConsent tablets, etc);
• Investigational Product : responsible for overall study reconciliation of IP
• Vendor Oversight : Assist with selection of vendors; Create and manage Vendor Oversight Plan for each vendor; review vendor contracts, work orders and Change Orders; day to day oversight of vendors
• Establish Review Committees : creating charter, assisting with member selection, contracting as needed, updating Annual Plan
• Site Closure Strategy : develop site closure plan
• Patient Recruitment Strategy : assist Project Managers in development of patient recruitment strategy and plan; develop recruitment materials; drive strategies for needing new sites
• Trial Master File : support customization of study/country/site specific docs; upload documents, reference Master File Index; oversight of TMF health; TMF reconciliation; TMF archival; quarterly TMF review
• Risk Management : initial Risk Assessment