Home › Companies › Parexel › Senior Study Contract Manager - FSP
Senior Study Contract Manager - FSP
Parexel · Netherlands-Remote · Remote · Active · Workday Recruiting
Job facts
| Field | Value |
|---|---|
| Company | Parexel |
| Title | Senior Study Contract Manager - FSP |
| Normalized title | - |
| Department / team | - |
| Location | Netherlands |
| Work model | Remote / Remote |
| Employment type | Full Time |
| Salary | - |
| Status | active |
| ATS provider | Workday Recruiting |
| Posted / first seen | 2026-06-05 / 2026-05-30 |
| Changed / last seen | 2026-06-06 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Parexel. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through Workday Recruiting. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| Work model jobs | Active Remote postings. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Parexel |
| Source | a38f5933-8d87-4b90-bb56-84b4c1881427 |
| ATS provider | Workday Recruiting |
Description
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Typical Accountabilities
· Adapt global templates of agreements to local use in accordance with local requirements and SOPs.
· Develop and negotiate clinical site budgets based on Fair Market Value.
· Negotiate agreement language and budget with clinical study sites.
· Act as point of contact and interface with Legal if necessary to ensure integrity of contracts.
· For each agreement maintain the status of agreement, budgets, issues, payments, any amendments for the duration of the study, and communications with internal and external sources.
· Ensure final contract documents are consistent with agreements reached at negotiations.
· Ensure all agreements are executed in a timely manner contributing to efficient site start-up timelines.
· Support internal and external audits activities.
· Ensure compliance with client ’s Code of Conduct and company policies and procedures relating to people, finance, technology and security.
· Ensure that all contracts are included in the TMF
Upon local decision, additional responsibilities may include*:
· Training and mentoring of new members of the local Study Team regarding financial/contractual issues and sharing experiences.
· Support preparation and negotiation of a Local Master Service Agreement
· Contribute to process improvements, knowledge transfer and best practice sharing. *Note: Additional responsibilities may be adjusted locally
Education, Qualifications, Skills and Experience
Essential
· Bachelor degree in related discipline, preferably in life science, law, finance or equivalent qualification.
· 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.
· Excellent attention to details.
· Good written and verbal communication skills.
· Good collaboration and interpersonal skills.
· Good negotiation skills.
· Ability to travel nationally/internationally as required.
Desirable
· Ability to work in an environment of remote collaborators.
· Post-graduate training in contracts administration or work experience as a paralegal in pharmaceutical or health care industry
· Manages change with a positive approach for self, team and the business. Sees change as an opportunity to improve performance and add value to the business.
· Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with reduced budget and in less time.
· Good analytical and problem-solving skills.
· Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines.
· Familiar with risk-based monitoring approach including remote monitoring.
· Good cultural awareness.
· Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an e-enabled environment.
· Team oriented and flexible; ability to respond quickly to shifting demands and opportunities.
· Good medical knowledge and ability to learn relevant client’s Therapeutic Areas.
Key stakeholders and relationships
Internal (to client or team)
· LSADs and Local Study Teams
· Line Manager and local SMM LT
· Clinical Quality Associate Director
· Local Medical Teams: MSLs and Medical Affairs
· Global Study Teams
· Global Clinical Solutions functions
· Clinical Data Management
· Regulatory Affairs
· Patient Safety
External (to client )
• Investigators and site personnel
• Study related vendors
• Inspectors
Full job record
| Job ID | b96ff37e5f6e78bcff23cfa78ac76cae73a1aeb3 |
| Org ID | 0c6955f0-4e0e-43b2-98b7-c020651fe1bc |
| Source ID | a38f5933-8d87-4b90-bb56-84b4c1881427 |
| Board ID | a38f5933-8d87-4b90-bb56-84b4c1881427 |
| Provider | workday |
| Provider Job Key | /job/Netherlands-Remote/Senior-Study-Contract-Manager---FSP_R0000042102 |
| Title | Senior Study Contract Manager - FSP |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Netherlands-Remote |
| Department | — |
| Team | — |
| Employment Type | full_time |
| Workplace Type | remote |
| Remote Policy | remote |
| Country | Netherlands |
| Region | — |
| City | — |
| Salary Raw | — |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://wd1.myworkdaysite.com/recruiting/parexel/Parexel_External_Careers/job/Netherlands-Remote/Senior-Study-Contract-Manager---FSP_R0000042102 |
| Apply URL | https://wd1.myworkdaysite.com/recruiting/parexel/Parexel_External_Careers/job/Netherlands-Remote/Senior-Study-Contract-Manager---FSP_R0000042102 |
| First Seen At | 2026-05-30 06:03:30Z |
| Last Seen At | 2026-06-06 09:44:42Z |
| Last Checked At | 2026-06-06 09:44:42Z |
| Last Changed At | 2026-06-06 09:44:42Z |
| Inactive At | — |
| Source Posted At | 2026-06-05 00:00:00Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=workday/board=wd1.myworkdaysite.com|parexel|Parexel_External_Careers/date=2026-06-06/2026-06-06T09-44-03-769Z-d8971a44a3c4aa5e8991760bf3f97217cce82940a3203cd02265c8253b6dbb66.json |
Event Fields
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"jobDescription": "<p><b>When our values align, there's no limit to what we can achieve.</b><br /> <br />At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.</p><p>Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.</p><p></p><p></p><p><span><b>Typical Accountabilities</b> </span></p><p><span>· Adapt global templates of agreements to local use in accordance with local requirements and SOPs. </span></p><p><span>· Develop and negotiate clinical site budgets based on Fair Market Value. </span></p><p><span>· Negotiate agreement language and budget with clinical study sites. </span></p><p><span>· Act as point of contact and interface with Legal if necessary to ensure integrity of contracts. </span></p><p><span>· For each agreement maintain the status of agreement, budgets, issues, payments, any amendments for the duration of the study, and communications with internal and external sources. </span></p><p><span>· Ensure final contract documents are consistent with agreements reached at negotiations. </span></p><p><span>· Ensure all agreements are executed in a timely manner contributing to efficient site start-up timelines. </span></p><p><span>· Support internal and external audits activities. </span></p><p><span>· Ensure compliance with </span><span>client</span>’s Code of Conduct and company policies and procedures relating to people, finance, technology and security. </p><p><span>· Ensure that all contracts are included in the TMF </span></p><p><span> </span></p><p><span><b>Upon local decision, additional responsibilities may include*:</b> </span></p><p><span>· Training and mentoring of new members of the local Study Team regarding financial/contractual issues and sharing experiences. </span></p><p><span>· Support preparation and negotiation of a Local Master Service Agreement </span></p><p><span>· Contribute to process improvements, knowledge transfer and best practice sharing. *Note: Additional responsibilities may be adjusted locally </span></p><p><span> </span></p><p><span><b>Education, Qualifications, Skills and Experience</b> </span></p><p><span><b><u>Essential</u></b> </span></p><p><span>· Bachelor degree in related discipline, preferably in life science, law, finance or equivalent qualification. </span></p><p><span>· Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP. · Good knowledge of relevant local regulations. </span></p><p><span>· Basic understanding of the drug development process. </span></p><p><span>· Good understanding of Clinical Study Management including monitoring, study drug handling and data management. </span></p><p><span>· Excellent attention to details. </span></p><p><span>· Good written and verbal communication skills. </span></p><p><span>· Good collaboration and interpersonal skills. </span></p><p><span>· Good negotiation skills. </span></p><p><span>· Ability to travel nationally/internationally as required. </span></p><p><span><b><u>Desirable</u></b> </span></p><p><span>· Ability to work in an environment of remote collaborators. </span></p><p><span>· Post-graduate training in contracts administration or work experience as a paralegal in pharmaceutical or health care industry </span></p><p><span>· Manages change with a positive approach for self, team and the business. Sees change as an opportunity to improve performance and add value to the business. </span></p><p><span>· Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with reduced budget and in less time. </span></p><p><span>· Good analytical and problem-solving skills. </span></p><p><span>· Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines. </span></p><p><span>· Familiar with risk-based monitoring approach including remote monitoring. </span></p><p><span>· Good cultural awareness. </span></p><p><span>· Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an e-enabled environment. </span></p><p><span>· Team oriented and flexible; ability to respond quickly to shifting demands and opportunities. </span></p><p><span>· Good medical knowledge and ability to learn relevant </span><span>client’s</span> Therapeutic Areas. </p><p><span> </span></p><p><span><b>Key stakeholders and relationships</b> </span></p><p><span><b><u>Internal (to </u></b></span><span><b><u>client</u></b></span><b><u> or team)</u></b> </p><p><span>· LSADs and Local Study Teams </span></p><p><span>· Line Manager and local SMM LT </span></p><p><span>· Clinical Quality Associate Director </span></p><p><span>· Local Medical Teams: MSLs and Medical Affairs </span></p><p><span>· Global Study Teams </span></p><p><span>· Global Clinical Solutions functions </span></p><p><span>· Clinical Data Management </span></p><p><span>· Regulatory Affairs </span></p><p><span>· Patient Safety </span></p><p><span> </span></p><p><span><b><u>External (to </u></b></span><span><b><u>client</u></b></span><b><u>)</u></b> </p><p><span>• Investigators and site personnel </span></p><p><span>• Study related vendors </span></p><p><span>• Inspectors </span></p>",
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