Site Contract Analyst
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Job Description
Contract Analyst supporting biotech companies in clinical development and start-up contracting activities. Collaborating with sponsors and ensuring compliance with project timelines.
Responsibilities:
- Support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs
- Develop simple investigator grant estimates and proposal text to support the proposal development process
- Utilize and maintain contract and budget templates and contracting systems, tools, processes, and training materials for selected sponsors
- Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries
- Provide specialist operational and financial contracting support to facilitate business development and clinical trials
- Assist in the creation and/or review of core scientific, technical and administrative documentation
- Contribute to the collection, interpretation, analysis and dissemination of contracting intelligence
- Ensure overall contracting efficiency and adherence to project timelines and financial goals
- Comply with contract management and quality standards
- Provide administrative and operational support to investigator site contract analysts, managers and directors
- Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans
Requirements:
- Bachelor's Degree in life sciences or health care
- 3 - 5 years relevant experience, including demonstrable experience acting as a contract negotiator
- Relevant sponsor or clinical research organization clinical site contracting experience
- Good negotiating and communication skills
- Good interpersonal skills and a strong team player
- Strong technical writing skills
- Understanding of regulated clinical trial environment and knowledge of drug development process
- Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
- Knowledge of applicable regulatory requirements, SOPs and company’s Corporate Standards
- Good organizational and planning skills
- Strong knowledge of Microsoft Office and e-mail applications
- Ability to interpret pricing models and to prepare proposals, bid grids and budgets
- Good understanding of clinical trial contract management
- Ability to establish and maintain effective working relationships with co-workers, managers and sponsors.
Benefits:
- Competitive salary
- Health insurance
- 401(k) matching
- Flexible work hours
- Paid time off
- Professional development opportunities
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