Biogen

Biogen

Manager, Site Contracts Management

Remote, USA

Sponsorship not specified$122k-$163kDetected 4 days ago
GCPProject ManagementNegotiationExcelContract ManagementClinical TrialsFDA RegulatoryResearchCommunicationPublic SpeakingOrganizational Skills

About the role

  • As the Manager, Site Contracts Management, you will play a pivotal role in the execution of Clinical Trial Agreements between our company and study sites, ensuring seamless conduct of global clinical trials.
  • Your responsibilities will span from the study planning stage through the lifecycle of the clinical trial, maintaining oversight of CROs to ensure compliant and timely execution of site contracts and payments across multiple regions.

Responsibilities

  • Provide consistent site contract global strategy, oversight, and support at the study level for all operating models on assigned studies.
  • Develop and maintain oversight of CROs to ensure compliant and timely execution of site contracts and payments.
  • Support in-house site contract development and negotiation as necessary.

Requirements

  • You are a proactive communicator, seamlessly liaising between internal and external teams to ensure clarity and compliance.
  • Required Skills:

Nice to have

  • Bachelor's Degree required
  • MBA/MPA/MPH/JD (or equivalent) preferred but not required.
  • Preferred Skills:

Skills

  • 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.
  • Experience in related areas of clinical operations, such as site start-up management or regulatory affairs.
  • Familiarity with global clinical trial agreements and scientific research collaborations.
  • Bachelor's Degree required; MBA/MPA/MPH/JD (or equivalent) preferred but not required.
  • Job Level: Management
  • Additional Information
  • The base compensation range for this role is: $122,000.00-$163,000.00

Compensation

  • Tuition reimbursement of up to $10,000 per calendar year

Benefits

  • Medical, Dental, Vision, & Life insurances
  • Fitness & Wellness programs including a fitness reimbursement
  • Paid Maternity and Parental Leave benefit
  • 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)
  • Employee stock purchase plan
  • Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.

Company info

  • Up to 12 company paid holidays + 3 paid days off for Personal Significance
  • 401(k) program participation with company matched contributions
  • We are a global team with a commitment to excellence, and a pioneering spirit.
  • As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact.
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