Manager, Site Contracts Management

Biogen

Manager of Site Contracts Management at Biogen ensuring execution of clinical trial agreements. Support for Phase I-IV clinical trials and scientific research collaborations with contract oversight.

Posted 7/18/2026full-timeRemote • 🇺🇸 United StatesMid-LevelSenior💰 $122,000 - $163,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in site contract negotiation and management within the biotechnology and pharmaceutical industries, ensuring compliance with GCP, ICH standards, and FDA/EMA guidelines. Proven ability to facilitate communication and collaboration between study sites and internal teams while providing strategic oversight and support.

Highest-signal resume keywords

Site Contract NegotiationProject ManagementGCP ComplianceBiotechnology Industry ExperienceConflict Resolution

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Site Contract DevelopmentBudget NegotiationClinical Trials ExecutionPhase I-IV ExperienceRegulatory Guidelines Understanding

Soft Skills

Excellent Negotiation SkillsDecision-Making SkillsPresentation SkillsStrong Organizational Skills

Certifications & Qualifications

Bachelor's DegreeMBA/MPA/MPH/JD Preferred

Industry Keywords

BiotechnologyPharmaceuticalCRO OversightClinical TrialsICH Standards

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Provide consistent site contract global strategy, oversight, and support at the study level for all operating models on assigned studies.
Serve as an escalation point for language issues from CROs and liaise with R&D Legal to resolve complex negotiations.
Contribute to department and cross-functional process development and improvements.
Develop and maintain oversight of CROs to ensure compliant and timely execution of site contracts and payments.
Provide strategic input on country-level contracts strategy as a regional SME.
Support in-house site contract development and negotiation as necessary.
Monitor trends and contribute to the refinement of existing guidance, tools, and templates.
Facilitate communication between study sites and internal teams to ensure alignment and compliance.
Ensure adherence to GCP, relevant ICH standards, and FDA/EMA guidelines.
Conduct presentations and provide training on site contracts best practices.

Requirements

What you’ll need

Bachelor’s degree
6+ years’ experience in the biotechnology/pharmaceutical industry within the site contracting outsourcing space.
Fully proficient in project management and site contract and budget negotiation and execution across Phase I-IV clinical trials.
Thorough understanding of GCP, relevant ICH standards, and FDA/EMA guidelines.
Excellent negotiation skills, conflict resolution, decision-making skills, and presentation skills.
Strong organizational skills, including the ability to prioritize needs and handle a high volume of tasks within a given timeframe.
Bachelor’s Degree required; MBA/MPA/MPH/JD (or equivalent) preferred but not required.

Benefits

Comp & perks

Medical, Dental, Vision, & Life insurances
Fitness & Wellness programs including a fitness reimbursement
Short- and Long-Term Disability insurance
A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
Up to 12 company paid holidays + 3 paid days off for Personal Significance
80 hours of sick time per calendar year
Paid Maternity and Parental Leave benefit
401(k) program participation with company matched contributions
Employee stock purchase plan
Tuition reimbursement of up to $10,000 per calendar year
Employee Resource Groups participation