12 publicaciones de empleo destacadas de study start up lead en spain (¡Están contratando!)

Associate Director, Functional Service Partnership (FSP), Site Contracts
Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Inglés
- Investigación
- Máster
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Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Microsoft Word
- Microsoft Excel
- Inglés
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Senior/Principal Clinical Team Manager, Hematology/Oncology
Thermo Fisher Scientific —En remoto
- Jornada completa
- Teletrabajo
- Microsoft Word
- Microsoft Excel
- Inglés
8d
Statistical Science Associate Director
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Doctorado
- Máster
English Faculty Member
Verto Education —Sevilla, Sevilla provincia
- Jornada completa
- Doctorado
- Inglés
- Máster
Solicitud rápida
Business Development Representative DACH
360Learning —En remoto
- Jornada completa
- Teletrabajo
- Ventas
- Salesforce
- Inglés
- Teletrabajo opcional
Automation Process Engineer
Basquevolt —Vitoria-Gasteiz, Álava provincia
- Español
- Inglés
- Ensamblaje
- Seguro de vida
Solicitud rápida
7d
Global Development Medical Director, Hematology Oncology
AstraZeneca —Barcelona, Barcelona provincia
- Horas extra
- Microsoft Excel
- Investigación
- Habilidades de comunicación
- Seguro oftalmológico
Sales Advisor Intern - English Speaker
ALPADIA Language Schools SA —Barcelona, Barcelona provincia
- Jornada completa
- Ventas
- Inglés
- Microsoft Office
Solicitud rápida
3d
Principal AI Engineer - Evinova
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Informática
- Oficina
3d
Study Start Up Lead
Rho Inc —España
- Jornada completa
- Teletrabajo
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Solicitud rápida
Lead Clinical Research Associate
United Biosource Corporation —España
- Teletrabajo
- Inglés
- Microsoft Office
- Grado
Solicitud rápida
9d

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Associate Director, Functional Service Partnership (FSP), Site Contracts
Thermo Fisher Scientific —En remoto
Process improvement and standardization: Establish and refine standards, templates, guidance, and tools for budgets and CSAs; identify opportunities for…

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Associate Director, Functional Service Partnership (FSP), Site Contracts

Thermo Fisher Scientific -
En remoto

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Detalles del empleo

Jornada completa

Cualificaciones

Investigación clínica
Inglés
Investigación
Máster
Project management
Grado
Gestión de conflictos
Liderazgo
Negociación

Descripción completa del empleo

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Role Description:

The Associate Director, Functional Service Partnership (FSP), Site Contracts is a full FTE member of the global study team for a Sponsor and serves as the central operational subject matter expert for clinical contracting and study budgets. The role provides end‑to‑end budget oversight from Clinical Study Protocol (CSP) development through study set‑up, maintenance, close‑out, and archiving. The FSP SITE CONTRACTS AD ensures application of country‑level Fair Market Value (FMV) at study and country level, maintains the master study and country budgets, and drives timely distribution of approved country budgets to Site Management and Monitoring /country organizations. As portfolio SME and CSA (Clinical Study Agreements) point‑of‑contact (POC) for Sponsor Study Management & Monitoring and Sponsor Legal, the role leads ongoing and ad hoc reviews of CSAs and budgets resulting from protocol amendments, ensures a complete, audit‑ready repository of signed CSAs and related documentation, and aligns cross‑study and portfolio budgets. The FSP SITE CONTRACTS AD partners across Study Management, Site Management & Monitoring (SMM), Legal, Procurement, Finance, and if needed external providers to deliver to scope, quality, budget, and timelines in line with ICH GCP, Sponsor SOPs, policies, and values.

Accountabilities:

Contracts and budget strategy and oversight: Set up and lead the end-to-end operational strategy for study contracting and budgeting across assigned studies and programs, aligning with CSP, country requirements, biosampling plans, and funding envelopes. Serve as the single point of accountability for budget integrity and contract alignment from concept to closeout.‑to‑end operational strategy for study contracting and budgeting across assigned studies and programs, aligning with CSP, country requirements, ‑out.
FMV governance and application: Ensure country level FMV benchmarks are established, current, and consistently applied across study and country budgets, including sites, central/specialty labs, and other vendors. Document FMV methodologies, justifications, and deviations in accordance with compliance and regulations. Level FMV benchmarks are established, current, and consistently applied across study and country budgets, including sites, central/specialty labs, and other vendors. Document FMV methodologies, justifications, and deviations in accordance with compliance and anti‑kickback regulations.
Master study and country budgets and CSA templates: Build, maintain, and own the master study and country budget and CSA templates; perform scenario modelling and sensitivity analysis based on study design changes, enrolment dynamics, and operational assumptions.
Budget and CSA distribution to countries: Finalize and distribute approved country budgets to SMM/country teams with clear negotiation guidance, parameters, and change control rules. Track implementation and provide clarification during site negotiations as needed. Maintains country study templates and adjusting changes in due course of the study as needed.
CSA subject matter expertise: Act as portfolio SME and primary POC for Clinical Study Agreements (CSAs) with SMM and Legal. Guide terms, rate structures, study specific appendices, and change orders; coordinate review cycles and approvals to meet startup timelines.‑specific appendices, and change orders; coordinate review cycles and approvals to meet start‑up timelines.
Protocol amendment impact assessment: Lead ongoing and ad hoc CSA and budget reviews triggered by protocol amendments or operational changes. Quantify impacts, secure approvals, adjust master and country budgets, and execute contract amendments in a timely and compliant manner.
Documentation ownership and repository management: Ensure timely maintenance and distribution of contracting documentation, including a complete, version controlled repository of signed CSAs, amendments, rate cards, and budget approvals across the portfolio; ensure eTMF completeness and inspection readiness.‑controlled repository of signed CSAs, amendments, rate cards, and budget approvals across the portfolio; ensure eTMF completeness and inspection readiness.
Partner with Finance on forecasting, risk/opportunity management, and governance reporting, if needed.
Cross-functional leadership and collaboration: Coordinate deliverables across Study Teams, SMM, Legal, Procurement, Finance, and scientific functions; facilitate decision making, resolve issues, and drive alignment on budget and contract priorities and timelines.‑functional leadership and collaboration‑making, resolve issues, and drive alignment on budget and contract priorities and timelines.
Process improvement and standardization: Establish and refine standards, templates, guidance, and tools for budgets and CSAs; identify opportunities for automation and AI enabled solutions; lead or contribute to continuous improvement and change initiatives impacting contracting and budgeting operations.‑enabled solutions; lead or contribute to continuous improvement and change initiatives impacting contracting and budgeting operations.
Training and enablement: Provide targeted training to Study Management, SMM, and cross functional teams on budget/CSA processes, FMV application, and change control; collect and share lessons learned and best practices.‑functional teams on budget/CSA processes, FMV application, and change control; collect and share lessons learned and best practices.

Required Education, Qualifications, Skills and Experience:

University degree (or equivalent)
At least 5 years of relevant clinical experience in the pharmaceutical industry, including 2+ years of site budget and contracts oversight/project management experience.
Extensive knowledge of clinical research regulatory requirements; excellent understanding of ICH/GCP, and study management processes, including contracting and study budget management.
Strong leadership and cross-functional collaboration skills with demonstrated ability to influence without authority and coordinate complex workstreams across scientific and operational functions.
Proven oversight/project management skills, including planning, risk management, timeline and budget oversight; proficiency with standard project tools and IT systems.
Excellent communication, stakeholder management, and relationship-building skills; strong negotiation and conflict management capabilities.
Strong organizational and problem-solving skills; ability to manage competing priorities and maintain attention to detail.
Fluent verbal and written English.

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