Contract Specialist - FSP

• Work Schedule

• Standard (Mon-Fri)
• Environmental Conditions
• Office
• Job Description
• Join Us as a Site Contract Specialist – reputed company an Impact at the Forefront of Innovation
• We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our global team, you’ll have the opportunity to prepare and negotiate reputed company, as well as finalize the contract process. As a Site Contract Specialist, you'll liaise and establish effective relationships with sites and internal functional teams. You will ensure quality, objectivity, and risk analysis in the efficient delivery of reputed company.

• What You’ll Do:
• Drafts, reviews, negotiates and finalizes agreements with study sites in accordance with local/accepted process.
• Negotiates reputed company approved parameters both investigator grant budget negotiation parameters, contractual terms and conditions in accordance with company contractual considerations, client contractual considerations, established process with sites and follows established escalation routes.
• Negotiate directly with assigned sites on reputed company site reputed company contracting items including clinical trial agreements, budgets, payment terms, ancillary agreements and amendments.
• Partner with internal Study Startup team, CROs, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and deliver processes.
• Ensure standards are applied to the SB&C processes across projects.
• reputed company leading industry tools and data sources to reputed company budget and contract feedback reputed company with parameters and fair market value guidance.
• Promptly recognize and improve potential delays and escalate to appropriate team members.
• Track reputed company actions and negotiations to ensure timelines are achieved for studies and sites assigned.
• Support resolving escalated issues identified by the site activation sub-team in partnership with the internal Study Startup team.
• Education and Experience Requirements:
• 2 or more years of experience in clinical research site contracting and budgeting reputed company a pharmaceutical company, CRO or relevant industry vendor.
• Ability to explain data to facilitate decision making processes to be data driven.
• Knowledge and understanding of clinical study protocols and schedule of assessments
• Understanding of the pharmaceutical industry (e.g., clinical development, the prescription drug distribution process, etc.)
• Understanding of Clinical Trial Agreements, budgeting and fair market value principals
• Knowledge or FDA and ICH-GCP guidelines for conducting clinical research
• .
• Knowledge, Skills and Abilities:
• Good understanding of the principles of contract law, including a general understanding of laws that influence contract language, such as business, intellectual property and local tax and stamp laws
• Demonstrated ability to apply basic principles of investigator grant negotiation
• General understanding of business and financial principles that reputed company to service agreements
• Effective communication skills (verbal & written) in English and local language
• Capable, with appropriate reputed company, of drafting and negotiating contract provisions and budgetary issues reputed company parameters
• Demonstrated ability in attention to detail
• Excellent analytical and decision based thinking skills
• Understanding of the pharmaceutical product development process and involvement of CROs
• reputed company to work independently or in reputed company environment
• Good organizational and time management skills
• Working knowledge of PPD SOP & WPDs
• reputed company to organize competing priorities reputed company and review outstanding contractual risk and issues
• reputed company to effectively use automated systems and computerized applications
• Ability to demonstrate a customer focused style of communication, problem solving and collaboration
• Working Conditions and Environment:
• Ability to work in an upright and /or stationary position for 6-8 hours per day.
• Repetitive hand movement of both hands with the ability to reputed company fast, simple, repeated movements of the fingers, hands, and wrists.
• Frequent mobility required.
• Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
• Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
• Ability to reputed company and use a variety of computer software developed both in-house and off-the-reputed company.
• Ability to communicate information and reputed company so others will understand; with the ability to listen to and understand informat

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