Investigator reputed company reputed company/Site reputed company reputed company
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At reputed company, we reputed company reputed company the reputed company goal - to improve the world's health. From reputed company to regulatory, consulting, and market reputed company, every clinical development solution we reputed company is underpinned by something special - a deep conviction in reputed company do.
reputed company of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we're committed to making a difference.
REMOTE POSITION- US
Key Accountabilities:
Contracting deliverables
Exercise good judgment in balancing the risks to the reputed company in making budget and contractual reputed company against the impacts to reputed company clinical trial timelines
Follow reputed company processes to reputed company, negotiate, reputed company and execute global clinical study agreements with institutions and investigators participating in sponsored reputed company
Work with partners to reputed company and reputed company 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 reputed company the reputed company division approved parameters
reputed company study level site contracting activities, reputed company other ICL and reputed company as primary study reputed company of contract for site contracting issues and timelines on assigned studies
Partner with reputed company and other divisions to manage escalations in the site budgeting and contracting reputed company
Partner with reputed company, Finance, pCRO and other divisions to identify and implement areas of improvement in the site contracting reputed company
Applies acquired job skills and procedures to complete substantive assignments, reputed company and tasks of moderate scope and complexity in applicable discipline
Collaboration
reputed company and reputed company relationships with key investigational sites and Site Management Organizations across the contracting and budgeting reputed company
Collaborates with invoicing specialists and/or invoice service provider to ensure alignment with Investigative Site contracting and compensation requirements
Interacts with clinical site reputed company & reputed company contacts, reputed company and partner reputed company 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 reputed company. Applies technical skills and discipline knowledge to contribute to achievement of reputed company business objectives
Compliance with reputed company 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 reputed company processes, ICH-GCPs and other applicable requirements
Skills:
Balance of general business, compliance, finance, reputed company, and drug development experience • Precise communications and presentation skills
Ability to plan, identify and mitigate risks to site contacting timelines
Ability to reputed company by influence rather than positional power to accomplish critical deliverables • reputed company in working in a highly reputed company based organization
reputed company 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
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