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HomeCompaniesParexelSenior Study Contract Manager - FSP

Senior Study Contract Manager - FSP

Parexel · Netherlands-Remote · Remote · Active · Workday Recruiting

Job facts

FieldValue
CompanyParexel
TitleSenior Study Contract Manager - FSP
Normalized title-
Department / team-
LocationNetherlands
Work modelRemote / Remote
Employment typeFull Time
Salary-
Statusactive
ATS providerWorkday Recruiting
Posted / first seen2026-06-05 / 2026-05-30
Changed / last seen2026-06-06 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Parexel.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through Workday Recruiting.Open
Provider filtered searchThe same provider as a filtered job collection.Open
Work model jobsActive Remote postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyParexel
Sourcea38f5933-8d87-4b90-bb56-84b4c1881427
ATS providerWorkday 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 IDb96ff37e5f6e78bcff23cfa78ac76cae73a1aeb3
Org ID0c6955f0-4e0e-43b2-98b7-c020651fe1bc
Source IDa38f5933-8d87-4b90-bb56-84b4c1881427
Board IDa38f5933-8d87-4b90-bb56-84b4c1881427
Providerworkday
Provider Job Key/job/Netherlands-Remote/Senior-Study-Contract-Manager---FSP_R0000042102
TitleSenior Study Contract Manager - FSP
Normalized Title
Statusactive
Activeyes
Location TextNetherlands-Remote
Department
Team
Employment Typefull_time
Workplace Typeremote
Remote Policyremote
CountryNetherlands
Region
City
Salary Raw
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://wd1.myworkdaysite.com/recruiting/parexel/Parexel_External_Careers/job/Netherlands-Remote/Senior-Study-Contract-Manager---FSP_R0000042102
Apply URLhttps://wd1.myworkdaysite.com/recruiting/parexel/Parexel_External_Careers/job/Netherlands-Remote/Senior-Study-Contract-Manager---FSP_R0000042102
First Seen At2026-05-30 06:03:30Z
Last Seen At2026-06-06 09:44:42Z
Last Checked At2026-06-06 09:44:42Z
Last Changed At2026-06-06 09:44:42Z
Inactive At
Source Posted At2026-06-05 00:00:00Z
Source Updated At
Raw Payload Uris3://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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  "last_changed_at": "2026-06-06T09:44:42.579Z",
  "active_status": "active"
}
Parsed Structured
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  "location": {
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    "city": null,
    "region": null,
    "country": "Netherlands",
    "is_remote": true,
    "confidence": 0.8
  },
  "salary_max": null,
  "salary_min": null,
  "inferred_at": "2026-06-06T09:44:41.934Z",
  "launch_scope": {
    "reason": "workday_production_catalog",
    "included": true,
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      "city": null,
      "region": null,
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    },
    "countries": [
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    ]
  },
  "remote_policy": "remote",
  "salary_period": null,
  "workplace_type": "remote",
  "salary_currency": null
}
Extensions
{}
Native Structured
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    "jobDescription": "<p><b>When our values align, there&#39;s no limit to what we can achieve.</b><br /> <br />At Parexel, we all share the same goal - to improve the world&#39;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&#39;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>",
    "questionnaireId": "8a4ea2a2118710014cce04690bac0000",
    "timeLeftToApply": "23 days left to apply",
    "jobPostingSiteId": "Parexel_External_Careers",
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        "descriptor": "Netherlands"
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      "descriptor": "Netherlands-Remote"
    },
    "jobPostingEndDateAsText": "End Date: June 30, 2026"
  }
}
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