Global Site Contracts Specialist - Remote & Budget Leader

Emerald Clinical Trials Inc.; Singapore; Hybrid; SGD 70.000 - 110.000; Vollzeit

Benefits dieser Stelle

Competitive compensation

Flexible working (remote or hybrid)

Career development

Employee wellbeing

Global exposure

Collaborative culture

Zusammenfassung

Emerald Clinical Trials Inc. is seeking a Site Contracts Specialist to support negotiation, execution, and management of clinical trial agreements and budgets. You will collaborate with sponsors, investigative sites, legal teams, and internal stakeholders to ensure timely and compliant contracting across global studies.

The role emphasizes fast-paced start-up activities, adherence to regulatory requirements, and cross-functional collaboration within a reputable CRO environment.

Qualifikationen

• Bachelor's degree or equivalent in scientific, healthcare, legal, business, or related discipline.

Aufgaben

• Prepare, review, negotiate, and manage clinical trial agreements, amendments, and associated contract documentation.
• Develop, negotiate, and manage site budgets within approved sponsor parameters.
• Act as a primary liaison between sponsors, investigative sites, legal teams, and internal stakeholders regarding contract and budget activities.
• Ensure contracts and budgets are executed within agreed study timelines and project milestones.
• Maintain contract management systems, trackers, templates, and documentation to support compliance and transparency.
• Review contractual documents to ensure accuracy, completeness, and alignment with applicable regulations, sponsor requirements, and company policies.

Kenntnisse

Site contract negotiation

Budget management

ICH-GCP

Regulatory knowledge

Stakeholder management

Contract management

Ausbildung

Bachelor's degree in life sciences or related

Tools

CTMS

Microsoft Office

Jobbeschreibung

Emerald Clinical Trials Inc. is seeking a Site Contracts Specialist to support negotiation, execution, and management of clinical trial agreements and budgets. You will collaborate with sponsors, investigative sites, legal teams, and internal stakeholders to ensure timely and compliant contracting across global studies.

The role emphasizes fast-paced start-up activities, adherence to regulatory requirements, and cross-functional collaboration within a reputable CRO environment.