Senior Contracts and Budget Associate

Precision Medicine Group · South KoreaRemotosenior

En corto

▸Revisa, redacta y negocia acuerdos clínicos y presupuestos de sitios.
▸Coordina con equipos internos y patrocinadores en Norteamérica y Europa.
▸Destacado: Requiere experiencia específica en contratos de investigación clínica, con foco en CDA, CTA y presupuestos.

En ~1 minuto te damos: quién te entrevista, las preguntas probables con respuestas desde tu CV, y tu CV adaptado a esta vacante. Gratis, sin tarjeta.

¿Qué piden?

✓3 años de experiencia en redacción, revisión y negociación de contratos clínicos.
✓Experiencia en gestión y seguimiento del proceso contractual.
✓Formación universitaria o experiencia equivalente en gestión de contratos.
✓Conocimiento en CDA, CTA, CTA-A y presupuestos de sitios.
✓Experiencia previa en industria de biotecnología, farmacéutica o investigación clínica.
✓Capacidad para liderar interacciones con patrocinadores y centros clínicos.

¿No cumplís todo? Es lo normal — tu dossier gratis te dice qué gaps tenés y cómo cubrirlos en la entrevista.

Confidentiality Disclosure AgrClinical Trial Agreements (CTAAmendments (CTA-A)Vendor contractsSite budgetsContract managementInternal study teamsSponsorsContract filesDocument archiving

¿A quién escribirle en Precision Medicine Group?

Tu dossier gratis identifica a las personas que te entrevistarían — con su background, qué valoran y cómo escribirles para destacar antes de aplicar.

Position Summary: Review, draft, negotiate and track a variety of legal agreements including confidentiality disclosure agreements (CDA), initial clinical trial agreements (CTA), amendments to the clinical trial agreements (CTA-A), site budgets and other various types of documents. Will work closely with the Clinical Operations study team and play an administrative role to ensure deliverables are in alignment with defined project timelines and expectations. Essential functions of the job include but are not limited to: â¢ Prepare and negotiate Agreements/Amendments such as Confidentiality Disclosure Agreements (CDA), Clinical Trial Agreements (CTA) and Amendments (CTA-A), vendor contracts and site budgets. â¢ Lead interactions with the North American and European internal study teams, as applicable â¢ Lead interactions regarding the various agreements with the Site(s) â¢ Lead interactions regarding assigned agreements with the Sponsor(s) â¢ Work with supervisor and various internal/external stakeholders to resolve contractual issues. â¢ Ensure adhered to company policies, procedures, and contracting standards. â¢ Update relevant study team members and sponsors regarding the status of contract negotiations and execution. â¢ Coordinate execution of the agreements â¢ Support the maintenance of contract files and databases, including email and document archiving. â¢ Other duties as assigned. e. Non-Disclosure Agreements, Clinical Trial Agreements, etc. as well as management, â¢ control and tracking of the contract process. â¢ Experience in contract research, life science, biotech or pharmaceutical industry is preferred. Please mention the word **SUBSIDIZE** and tag RNTQuMjExLjE3NS4xOTA= when applying to show you read the job post completely (#RNTQuMjExLjE3NS4xOTA=). This is a beta feature to avoid spam applicants. Companies can search these words to find applicants that read this and see they're human.

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