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Investigator Contracts Lead/Site Contracts Lead
Parexel · Canada-Ontario-Remote; 2 Locations; Canada-Quebec-Remote · Remote · Active · Workday Recruiting
Job facts
| Field | Value |
|---|---|
| Company | Parexel |
| Title | Investigator Contracts Lead/Site Contracts Lead |
| Normalized title | - |
| Department / team | - |
| Location | Canada |
| Work model | Remote / Remote |
| Employment type | Full Time |
| Salary | - |
| Status | active |
| ATS provider | Workday Recruiting |
| Posted / first seen | 2026-06-04 / 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.
REMOTE POSITION- US Key Accountabilities:
Contracting deliverables
Exercise good judgment in balancing the risks to the client in making budget and contractual decisions against the impacts to client clinical trial timelines Follow client processes to develop, negotiate, track and execute global clinical study agreements with institutions and investigators participating in sponsored clinical trials Work with partners to develop and oversee the global site budget process Work with clinical trial sites and directly negotiate cost, business and contractual terms and conditions with investigators/institutions, making changes to contract templates within the Legal division approved parameters Lead study level site contracting activities, direct other ICL and act as primary study point of contract for site contracting issues and timelines on assigned studies Partner with Legal and other divisions to manage escalations in the site budgeting and contracting space Partner with Legal, Finance, pCRO and other divisions to identify and implement areas of improvement in the site contracting space Applies acquired job skills and procedures to complete substantive assignments, projects and tasks of moderate scope and complexity in applicable discipline
Collaboration
Lead and develop relationships with key investigational sites and Site Management Organizations across the contracting and budgeting interface Collaborates with invoicing specialists and/or invoice service provider to ensure alignment with Investigative Site contracting and compensation requirements Interacts with clinical site contracts & legal contacts, client and partner legal team, study management, site payments team, peer site contracting colleagues, CRO site contracting teams Contributes to design, development and implementation of major business initiatives or special projects. Applies technical skills and discipline knowledge to contribute to achievement of client business objectives
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:
Balance of general business, compliance, finance, legal, and drug development experience • Precise communications and presentation skills Ability to plan, identify and mitigate risks to site contacting timelines Ability to lead by influence rather than positional power to accomplish critical deliverables • Success in working in a highly matrix based organization Fluency in written and spoken English is required
Knowledge and Experience:
Experience with clinical study budgets and contracting negotiation principles, practices, processes, and activities Knowledge of the principles, concepts and theories in applicable business discipline Experience in drafting and negotiation of Clinical Trial Agreements with clinical trial sites in a global operation preferred
Education :
Bachelor’s Degree or equivalent and 5+ years of experience in clinical development operations or clinical trial outsourcing OR Juris Doctorate or equivalent and 2+ years of experience in clinical development operations or clinical trial outsourcing #LI-LG4
Full job record
| Job ID | 60db33544424fea4d05a280d210041c6fca8746d |
| 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/Canada-Ontario-Remote/Investigator-Contracts-Lead-Site-Contracts-Lead_R0000041275 |
| Title | Investigator Contracts Lead/Site Contracts Lead |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Canada-Ontario-Remote; 2 Locations; Canada-Quebec-Remote |
| Department | — |
| Team | — |
| Employment Type | full_time |
| Workplace Type | remote |
| Remote Policy | remote |
| Country | Canada |
| Region | — |
| City | — |
| Salary Raw | — |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://wd1.myworkdaysite.com/recruiting/parexel/Parexel_External_Careers/job/Canada-Ontario-Remote/Investigator-Contracts-Lead-Site-Contracts-Lead_R0000041275 |
| Apply URL | https://wd1.myworkdaysite.com/recruiting/parexel/Parexel_External_Careers/job/Canada-Ontario-Remote/Investigator-Contracts-Lead-Site-Contracts-Lead_R0000041275 |
| 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 | 2026-06-04 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 |
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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><div><b>REMOTE POSITION- US</b></div><div></div><div><div><div><div><p><b><u>Key Accountabilities:</u></b></p><p><b>Contracting deliverables</b></p><ul><li>Exercise good judgment in balancing the risks to the client in making budget and contractual decisions against the impacts to client clinical trial timelines</li><li>Follow client processes to develop, negotiate, track and execute global clinical study agreements with institutions and investigators participating in sponsored clinical trials</li><li>Work with partners to develop and oversee the global site budget process</li><li>Work with clinical trial sites and directly negotiate cost, business and contractual terms and conditions with <span>investigators/institutions,</span> making changes to contract templates within the Legal division approved parameters</li><li>Lead study level site contracting activities, direct other ICL and act as primary study point of contract for site contracting issues and timelines on assigned studies</li><li>Partner with Legal and other divisions to manage escalations in the site budgeting and contracting space</li><li>Partner with Legal, Finance, pCRO and other divisions to identify and implement areas of improvement in the site contracting space</li><li>Applies acquired job skills and procedures to complete substantive assignments, projects and tasks of moderate scope and complexity in applicable discipline</li></ul><p></p><p><b>Collaboration</b></p><ul><li>Lead and develop relationships with key investigational sites and Site Management Organizations across the contracting and budgeting interface</li><li>Collaborates with invoicing specialists and/or invoice service provider to ensure alignment with Investigative Site contracting and compensation requirements</li><li>Interacts with clinical site contracts & legal contacts, client and partner legal team, study management, site payments team, peer site contracting colleagues, CRO site contracting teams</li><li>Contributes to design, development and implementation of major business initiatives or special projects. Applies technical skills and discipline knowledge to contribute to achievement of client business objectives</li></ul><p></p><p><b>Compliance with Parexel standards</b></p><ul><li>Complies with required training curriculum </li><li>Completes timesheets accurately as required</li><li>Submits expense reports as required</li><li>Updates CV as required</li><li>Maintains a working knowledge of and complies with Parexel processes, ICH-GCPs and other applicable requirements</li></ul><p></p><p><b><u>Skills: </u></b></p><ul><li>Balance of general business, compliance, finance, legal, and drug development experience • Precise communications and presentation skills</li><li>Ability to plan, identify and mitigate risks to site contacting timelines</li><li>Ability to lead by influence rather than positional power to accomplish critical deliverables • Success in working in a highly matrix based organization</li><li>Fluency in written and spoken English is required</li></ul><p></p><p><b><u>Knowledge and Experience: </u></b></p><ul><li>Experience with clinical study budgets and contracting negotiation principles, practices, processes, and activities</li></ul><ul><li>Knowledge of the principles, concepts and theories in applicable business discipline</li><li>Experience in drafting and negotiation of Clinical Trial Agreements with clinical trial sites in a global operation preferred</li></ul><p></p><p><b><u>Education</u></b>:</p><ul><li>Bachelor’s Degree or equivalent and 5+ years of experience in clinical development operations or clinical trial outsourcing OR</li><li>Juris Doctorate or equivalent and 2+ years of experience in clinical development operations or clinical trial outsourcing</li></ul></div></div></div></div><p>#LI-LG4</p>",
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