MS OfficeCommunication SkillsNegotiationAttention to detailOrganizational skillsRelationship building
Requirements:
Graduate, postgraduate, 4-year college degree
Experience in a CRO/healthcare field
Minimum 5 years of experience in drafting, reviewing, and negotiating site Clinical Trial Agreements, Vendor Contracts and Site Budget negotiations.
Experienced leading interactions with Study Teams and Sponsor
Bachelors in law, scientific fields, business administration or equivalent degree (Preferred)
Excellent organizational and communication skills and attention to detail (Preferred)
Knowledgeable on setting up Contracting Plans - Guides for CTA & Budget negotiations (Preferred)
Successful handling relationship study team and/or with CRAs/Start-up Associate/(S)BSCA to meet study timelines (Preferred)
Proficient in MS Office software programs and computer applications
Works well independently and cooperatively with others to achieve common goals in a virtual environment.
Responsibilities:
Review, draft, and negotiate a variety of agreements including master services agreements, site contracts, consulting agreements, vendor agreements, confidentiality agreements, and other client contracts.
Work with supervisor and various internal/external key stakeholders to resolve/escalate contractual issues.
Ensure adherence to company policies, procedures, and contracting standards.
Update relevant study team members regarding the status of contract negotiations and execution.
Establish, track, report, and manage site contract metrics.
Support the maintenance of contract files and databases, including contract archiving.
Assist in designing and implementing policies and procedures to affect the timely execution of contracts.
Recognize where processes can be improved and take corrective action.