Site Contract Specialist
Thermo Fisher ScientificSalary not specified
Not SpecifiedCompensation
Mid-level (3 to 4 years)Experience Level
Full TimeJob Type
UnknownVisa
Healthcare, Medical DevicesIndustries
Requirements
- Associates Degree (≈ 13 years)
- Minimum 1 year related experience
- Preferred: Bachelor's Degree in Business Administration, a related field, or equivalent
- Preferred: Sponsor Pharma or Biotech experience
- Preferred: Direct knowledge of Sponsor Clinical Contracting
- Preferred: 5 years related work experience in Clinical contract/budget or equivalent combination of education & experience
- Preferred: Associate Bachelor's Degree in Business Administration, a related field, or equivalent and/or Paralegal certificate
- Negotiations skills in redlining documents and analytical experience or equivalent
- Familiarity with grant and contract requirements, policies, and procedures
- Knowledge of contract law and legal terminology
- Understanding of fundamental legal principles & terminology
- Knowledge of Clinical and AdvaMed Code of Ethics on Interactions with Health Care Professionals
- Knowledge and understanding of GCP, ICH, GLP and other federal, state, industry rules and regulations governing technical aspects of clinical grants and contracts
- Ability to ensure all required data from studies and sites complies with regulatory and government requirements (Sunshine Act, FWA, Human Subject Protection training, Clinical Insurance)
Responsibilities
- Under minimal guidance & supervision, develop & negotiate contracts, contract amendments and complex budgets with site partners within expected timelines/metrics
- Proactively collaborate with external/internal partners to address & resolve contract/budget issues to meet study milestones and deadlines
- Review informed consents to ensure alignment with contract/agreement and provide guidance to study teams
- Anticipate potential contract/budget compliance issues and timely risk mitigation
- Provides technical assistance in developing, negotiating, reviewing, and processing clinical study and research contracts and budgets
- Understands key business drivers and corporate clinical priorities; uses this understanding to accomplish own work
- Solves problems in straightforward situations; analyzes possible solutions using technical experience, judgment and precedents
- Impacts quality of own work and the work of others on the team; works within guidelines and policies
- Explains complex information to others in straightforward situations
- Capable of routine negotiations with little supervision
Skills
Contract Negotiation
Contract Review
Budget Processing
Clinical Study Contracts
Research Contracts
Technical Assistance
Abbott
Healthcare solutions in diagnostics and devices
About Abbott
Abbott Laboratories focuses on improving health through various medical technologies and health solutions. The company operates in areas such as cardiovascular health, diabetes management, diagnostic testing, nutrition, and neuromodulation for chronic pain and movement disorders. Abbott's products include advanced medical devices and diagnostic tests that help healthcare professionals and patients manage health conditions effectively. For example, their cardiovascular technologies assist in heart health management, while diabetes care products enable accurate glucose monitoring without painful fingersticks. Unlike many competitors, Abbott emphasizes accessibility and affordability in its offerings, aiming to make life-changing technologies available to a broader audience. The company's goal is to positively impact global health and well-being, supported by a commitment to sustainability and a 2030 Sustainability Plan.
Lake Bluff, IllinoisHeadquarters
1888Year Founded
IPOCompany Stage
HealthcareIndustries
10,001+Employees