Jobs.ca
Jobs.ca
Language
Parexel logo

Investigator Contracts Lead - FSP

Parexel6 days ago
Ontario
Senior Level

About the role

Primary Location: Canada, Ontario, Remote

Additional Locations: Canada, Alberta, Remote; Canada, Quebec, Remote

Job ID R0000034860

Category Clinical Trials

ABOUT THIS ROLE

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-LO1

#LI-REMOTE

About Parexel

Pharmaceutical Manufacturing
10,000+

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.

Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are:

• Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming.

We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.