The Senior Study Contract Manager (Sr.SCM) play an important role in driving the costings and contracts being responsible for negotiation and budgeting in clinical trials and for developing and managing contracts and annexes with investigators and institutions or external vendors ensuring ethical, fair, and compliant practices. Sr.SCM has regular communication with investigators and institutions as well as other key external and internal stakeholders.

Adapts global templates of agreements to local use in accordance with
local requirements and SOPs.
• Develops and negotiate clinical site budgets based on Fair Market
Value.
• Negotiates agreement language and budget with clinical study sites.
• Acts as point of contact and interface with Legal if necessary to ensure
integrity of contracts.
• For each agreement maintains the status of agreement, budgets, issues,
payments, any amendments for the duration of the study, and
communications with internal and external sources.
• Ensures final contract documents are consistent with agreements
reached at negotiations.
• Ensures all agreements are executed in a timely manner contributing to
efficient site start-up timelines.
• Supports internal and external audits activities.
• Ensures compliance with client’s Code of Conduct and company policies
and procedures relating to people, finance, technology, and security.
• Ensures that all contracts are included in the Trial Master File (TMF).
Upon local decision, additional responsibilities may include*:
Parexel International

Job Description
• Training and mentoring of new members of the local Study Team
regarding financial/contractual issues and sharing experiences.
• Supports preparation and negotiation of a Local Master Service
Agreement.
• Contributes to process improvements, knowledge transfer and best
practice sharing.
*Note: Additional responsibilities may be adjusted locally
Compliance with
Parexel standards • Complies with required training curriculum.
• Completes timesheets accurately as required.
• Submits expense reports as required.
• Updates CV as required.
• Maintains a working knowledge of and complies with Parexel processes,
ICH-GCPs and other applicable requirements.

Skills:
• Excellent attention to details.
• Good written and verbal communication skills.
• Good collaboration and interpersonal skills.
• Good negotiation skills.
• Read, write, and speak fluent English.
• Fluency in host country language required.

Knowledge and Experience:
• At lease 2-year experience in site contract negotiation/customization.
• Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP.
• Good knowledge of relevant local regulations.
• Basic understanding of the drug development process.
• Good understanding of Clinical Study Management including monitoring, study drug handling and
data management.

Education:
• Bachelor’s degree in related discipline, preferably in life science, law, finance, or equivalent
qualification.
Other:
• Ability to travel nationally/internationally as required.