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SUSUSONITY
Director, Head of Clinical Agreements (CA) - Sites and HCPs(m/w/x)
Eysins
Full-timeOn-siteSenior
Nejo AI Summary
Leading clinical trial agreement negotiations for oncology, neurology, and fertility medicines. 10+ years clinical research experience, including contract/budget negotiation, required. Master’s degree in law or paralegal studies preferred.
Requirements
- Minimum 10 years clinical research experience
- Focus on clinical trial contract/budget negotiation/management
- Master’s degree in related field
- Master’s degree preferably in law or paralegal studies
- In-depth knowledge of clinical trial regulations
- In-depth knowledge of contract law
- In-depth knowledge of industry standards (FDA, ICH-GCP, etc.)
- Strong leadership skills
- Ability to drive process improvements
- Excellent negotiation skills
- Excellent communication skills
- Ability to manage complex discussions effectively
- Skilled in developing strong working relationships
- Skilled in maintaining strong working relationships
- Skilled in working with internal and external stakeholders
- Proactive risk identification
- Proactive inefficiency identification
- Focus on operational excellence
- Commitment to fostering inclusion and belonging
Tasks
- Lead the team managing Site and HCP Agreements for Clinical Trials
- Provide strategic direction and coaching to the team
- Offer technical support to foster a collaborative environment
- Develop negotiation strategies for clinical agreements
- Ensure compliance with regulatory standards
- Drive process improvements for operational efficiency
- Oversee complex negotiations, including budget discussions
- Ensure timely and effective resolution of negotiation issues
- Account for execution, performance, and quality metrics of Clinical Agreements
- Identify trends and gaps affecting key deliverables
- Coordinate revisions of Master Clinical Site Agreement templates
- Update Legal Manuals and negotiation guidance documents
- Collaborate with internal and external partners on document revisions
- Contribute to the advancement of clinical research
Work Experience
- 10 years
Education
- Master's degree
Languages
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of SUSONITY and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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SUSUSONITY
Director, Head of Clinical Agreements (CA) - Sites and HCPs(m/w/x)
Eysins
Full-timeOn-siteSenior
Nejo AI Summary
Leading clinical trial agreement negotiations for oncology, neurology, and fertility medicines. 10+ years clinical research experience, including contract/budget negotiation, required. Master’s degree in law or paralegal studies preferred.
Requirements
- Minimum 10 years clinical research experience
- Focus on clinical trial contract/budget negotiation/management
- Master’s degree in related field
- Master’s degree preferably in law or paralegal studies
- In-depth knowledge of clinical trial regulations
- In-depth knowledge of contract law
- In-depth knowledge of industry standards (FDA, ICH-GCP, etc.)
- Strong leadership skills
- Ability to drive process improvements
- Excellent negotiation skills
- Excellent communication skills
- Ability to manage complex discussions effectively
- Skilled in developing strong working relationships
- Skilled in maintaining strong working relationships
- Skilled in working with internal and external stakeholders
- Proactive risk identification
- Proactive inefficiency identification
- Focus on operational excellence
- Commitment to fostering inclusion and belonging
Tasks
- Lead the team managing Site and HCP Agreements for Clinical Trials
- Provide strategic direction and coaching to the team
- Offer technical support to foster a collaborative environment
- Develop negotiation strategies for clinical agreements
- Ensure compliance with regulatory standards
- Drive process improvements for operational efficiency
- Oversee complex negotiations, including budget discussions
- Ensure timely and effective resolution of negotiation issues
- Account for execution, performance, and quality metrics of Clinical Agreements
- Identify trends and gaps affecting key deliverables
- Coordinate revisions of Master Clinical Site Agreement templates
- Update Legal Manuals and negotiation guidance documents
- Collaborate with internal and external partners on document revisions
- Contribute to the advancement of clinical research
Work Experience
- 10 years
Education
- Master's degree
Languages
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of SUSONITY and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
SUSONITY
Industry
Healthcare
Description
Das Unternehmen entwickelt Medikamente, intelligente Geräte und innovative Technologien in Therapiegebieten wie der Onkologie, Neurologie und Fruchtbarkeit.