Study Start-Up And Site Contracts Manager

in Healthcare + Life Sciences
  • New York, New York View on Map
  • Salary: $190.00 - $220,000.00
Permanent

Job Detail

  • Experience Level Sr Level
  • Degree Type Bachelor of Science (BS)
  • Employment Full Time
  • Working Type Remote
  • Job Reference 0000015330
  • Salary Type Annually
  • Industry Pharmaceuticals
  • Selling Points

    Lead impactful clinical trial start-up projects in a remote role. Collaborate with diverse teams to optimize oncology study processes. Enhance your expertise in regulatory compliance and contract management.

Job Description

Overview

  • Manage study start-up processes and site contract negotiations for clinical trials in oncology.
  • Collaborate with internal teams and external stakeholders to ensure timely site activation.
  • Analyze and resolve challenges in regulatory compliance and contract execution.
  • Develop workflows and standardize procedures to optimize study start-up efficiency.
  • Ensure adherence to regulatory guidelines and clinical trial methodologies.
  • Support IRB/EC submissions and review Informed Consent Forms for compliance.
  • Coordinate with vendors to achieve quality execution of start-up activities.
  • Provide guidance on protocol interpretation and study documentation to research sites.

Key Responsibilities & Duties

  • Negotiate clinical trial agreements with investigative sites ensuring favorable terms.
  • Collaborate across Clinical Development, Medical Affairs, and Regulatory Affairs for timely site start-up.
  • Evaluate priorities and adjust strategies to meet business needs effectively.
  • Identify and mitigate risks in study start-up processes proactively.
  • Lead internal study start-up team meetings and develop site initiation plans.
  • Ensure quality and compliance of Trial Master File documents during start-up.
  • Track and report site interaction status updates accurately and descriptively.
  • Support vendor performance oversight to achieve start-up timelines and quality.

Job Requirements

  • Bachelor’s Degree in Science or equivalent; legal background preferred.
  • Minimum 5 years of experience in study start-up and site contracts management.
  • Proven knowledge of clinical trial methodologies and regulatory guidelines.
  • Strong analytical skills for resolving study start-up challenges effectively.
  • Experience negotiating clinical trial agreements with research sites preferred.
  • Ability to manage multiple projects and meet study start-up milestones.
  • Excellent communication skills for interacting with diverse stakeholders.
  • Ability to work effectively in a matrixed environment and collaborate across teams.
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