Investigator reputed company reputed company - FSP

reputed company our values align, there's no limit to reputed company can reputed company. At reputed company, we reputed company reputed company the same goal - to improve the world's health. From clinical trials 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.

Each 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.

Key Accountabilities:

Contracting deliverables

• Exercise good judgment in balancing the risks to the client in making budget and contractual reputed company against the impacts to client clinical trial timelines
• Follow client processes to reputed company, negotiate, track and execute global clinical study agreements with institutions and investigators participating in sponsored clinical trials
• 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 Legal division approved parameters
• reputed company study level site contracting activities, direct other ICL and act as primary study reputed company 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 reputed company
• Partner with Legal, 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, projects 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 & 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 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, legal, 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 matrix 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

Originally posted on Himalayas