2. Review incoming agreements and amendments for accuracy and completeness.

3. Assists in preparation of information for distribution regarding contract status, compliance documentation, modifications, negotiations, and terminations.

4. Communicates assignments to negotiators, principal investigators, study teams, accounting, business administrators, and sponsors as needed.

5. Collaborates with research administration, compliance, finance, legal and other institutional departments to resolve contract-related issues.

6. Review, support negotiations, and conclude confidentiality agreements for research activities.

7. Finalize research agreements including securing signatures, oversee handoff of completed agreements to Principal Investigators for back end processing including initiating the account setup process.

8. Maintain accurate records regarding all contractual agreements.

9. Prepares special reports and analyses, as required.

1. High attention to detail and ability to multi-task

2. Works independently and displays initiative and sound judgement.

3. Ability to interact and communicate, both orally and in writing, with individuals from all levels within the organization is required.

4. Proficiency in MS Office Suite (Outlook, Word, Excel) is required.

5. Competency with the incorporation artificial intelligence (CoPilot, etc) into workflows is required

6. Preferred experience in clinical trial agreement administration and in a healthcare setting.

7. Minimum two years of research relevant experience preferred

Education and Experience

1. Education: Bachelor's degree in healthcare, business administration, or related field.

2. Licensure:

3. Certification:

4. Years of relevant experience: minimum 3 years is required.

5. Years of supervisory experience:  NA