Contracts Consultant

Redbock - an NES Fircroft company; Mahwah (NJ); Remote; USD 70,000 - 100,000; Part time

Job summary

Redbock - an NES Fircroft company seeks a Contracts Consultant to manage and negotiate clinical study site contracts and oversee related site payments.

The role emphasizes cross-functional communication with study sites, business, program management and accounting, leveraging strong Word skills and Medidata experience where applicable. This remote, 12-month assignment offers workload-based extension.

Qualifications

• Minimum 5 years in life sciences industry with contract exposure.
• 3 years negotiating clinical site contracts and handling site payments.
• Strong understanding of clinical trial execution and site involvement.

Responsibilities

• Negotiate terms and conditions of clinical trial site contracts.
• Communicate with study sites, business, program management and legal personnel.
• Review contracts for site payments and coordinate with accounting.
• Perform additional duties as needed.

Skills

Life sciences industry experience

Clinical site contract negotiation

Site payments processing

Communication with stakeholders

Education

Bachelor's Degree in Life Sciences or related field

Tools

Microsoft Word (Track Changes)

Medidata experience

Job description

CONTRACTS CONSULTANT (12-months, Potential for Extension based on workload/performance)

SUMMARY

Consultant needed for managing, negotiating and processing clinical study site contracts, and related site payments

DUTIES & RESPONSIBILITIES

• Contract negotiations for terms and conditions related to clinical trial sites
• Related written and verbal communications with study sites, business, program management, clinical operations and legal personnel
• Cross referencing contracts for terms and conditions related to site payments, and processing site payments in conjunction with accounting personnel
• Other duties, as required

QUALIFICATIONS & REQUIREMENTS

• 5 years of relevant life sciences industry experience
• 3 years of clinical site contract negotiation and site payment experience
• Solid overall understanding of clinical trial execution and study site involvement
• High-proficiency in Microsoft Word, including tracking document changes and proposed changes. Medidata experience is a plus
• Relevant Bachelor's Degree

LOCATION

Work can be performed remotely from home