Adriana Sandoval

• Accurately and with attention to detail leads and contributes to the timely development of high-quality contracts/agreements.
• Provides legal support and negotiates as needed contracts including but not limited to confidentiality agreements, Master Services Agreements, Clinical Trial Agreements with vendors, clients, consultants, and sites ensuring that the agreements are aligned with ProSciento’s interests.
• Drafts amendments with vendors, clients, consultants, and sites.
• Manages and resolves contracting issues between ProSciento and its clients, sites, vendors and other potential business partners/parties to a business agreement/contract.
• Responds to inquiries from sites, vendors, and sponsors professionally, efficiently, and effectively, and follows up with investigative sites and vendors concerning outstanding contracts and budgets on as-needed basis, and as frequently as necessary to resolve any concerns/issues as quickly as possible.
• Produces high-quality, error-free legal documents for final execution.
• Prioritizes daily activities according to importance and urgency.
• Manages documents from creation to completion.
• Maintains updated information of all study related information to use as reference in daily duties.
• Stays abreast of changes in studies and/or updates to study/project specific scope of work or client preferences.

· Fosters team building, positive communication, and corporate culture. Maintains a positive working environment, developing and maintaining excellent relationships with colleagues and clients.

• Manages, supports, and assists with a variety of administrative duties related to budgeting and contracting, under the direction of the Associate Director of Budgeting and Contracting

• Participate in administrative aspects of the screening process for in-house studies for human subject clinical research trials
• May be required to perform other duties (including subject recruitment and project management assistance) as needed

• Participate in administrative aspects of the screening process for in-house studies for human subject clinical research trials
• May be required to perform other duties (including subject recruitment and project management assistance) as needed