Minimum Qualifications:Bachelor's degree from an accredited institution.At least 5 years of relevant experience in drafting and negotiating Clinical Trial Agreements and site budgets.Experience in leading interactions with Study Teams and Sponsors.Preferred Qualifications:Degree in law, business administration, or a scientific field.Exceptional organizational and communication abilities with strong attention to detail.Knowledge of Contracting Plans and negotiation strategies for CTAs and budgets.Proven success in managing relationships with study teams and CRAs to meet study timelines.
About the job
Key Responsibilities:
Review, draft, and negotiate a range of agreements including clinical trial agreements, site contracts, budgets, and confidentiality agreements.
Collaborate with supervisors and stakeholders to address and resolve contractual issues.
Ensure compliance with company policies and contracting standards.
Provide regular updates to study team members regarding the progress of contract negotiations.
Establish and manage metrics related to site contracts.
Maintain and archive contract files and databases.
Contribute to the development and execution of policies to expedite contract execution.
Identify process improvement opportunities and implement corrective actions.
Perform additional duties as assigned.
About Precision Medicine Group
Precision Medicine Group is a leading organization dedicated to advancing the field of precision medicine through innovative research and clinical solutions. We focus on improving patient outcomes by leveraging cutting-edge science and technology.
This job posting is no longer active and is not accepting applications.
Minimum Qualifications:Bachelor's degree from an accredited institution.At least 5 years of relevant experience in drafting and negotiating Clinical Trial Agreements and site budgets.Experience in leading interactions with Study Teams and Sponsors.Preferred Qualifications:Degree in law, business administration, or a scientific field.Exceptional organizational and communication abilities with strong attention to detail.Knowledge of Contracting Plans and negotiation strategies for CTAs and budgets.Proven success in managing relationships with study teams and CRAs to meet study timelines.
About the job
Key Responsibilities:
Review, draft, and negotiate a range of agreements including clinical trial agreements, site contracts, budgets, and confidentiality agreements.
Collaborate with supervisors and stakeholders to address and resolve contractual issues.
Ensure compliance with company policies and contracting standards.
Provide regular updates to study team members regarding the progress of contract negotiations.
Establish and manage metrics related to site contracts.
Maintain and archive contract files and databases.
Contribute to the development and execution of policies to expedite contract execution.
Identify process improvement opportunities and implement corrective actions.
Perform additional duties as assigned.
About Precision Medicine Group
Precision Medicine Group is a leading organization dedicated to advancing the field of precision medicine through innovative research and clinical solutions. We focus on improving patient outcomes by leveraging cutting-edge science and technology.