<p>Job Title: Director of Clinical Trial Data Quality</p> <p>Job Description</p> <p>The Director of Clinical Trial Data Quality will be responsible for overseeing clinical research auditing across the consortium. This role involves supporting the Data Safety Monitoring Board/Committee, maintaining the Data Safety and Monitoring Plan, and implementing quality improvement processes. Additionally, the Director will ensure quality control of electronic Case Report Forms (eCRFs) and other Clinical Trial Management System (CTMS) data, while overseeing operational policies and procedures.</p> <p>Responsibilities</p> <ul> <li>Oversee clinical research auditing across the consortium. </li><li>Support the Data Safety Monitoring Board/Committee. </li><li>Maintain the Data Safety and Monitoring Plan. </li><li>Implement quality improvement processes. </li><li>Ensure quality control of eCRFs and CTMS data. </li><li>Oversee operational policies and procedures. </li></ul> <p>Essential Skills</p> <ul> <li>Proficiency in data quality management. </li><li>Experience with Data Safety Monitoring Boards (DSMB). </li><li>Expertise in clinical data management. </li><li>Strong understanding of clinical trials. </li></ul> <p>Additional Skills & Qualifications</p> <ul> <li>Experience in data quality and Data Safety Monitoring Board management. </li></ul> <p>Work Environment</p> <p>This position is 100% remote with quarterly onsite meetings. The Director will report to the Vice President of Clinical Research Management and will work within the Office of Data Quality. The role involves overseeing a team of 40-45 people.</p> <p>Job Type & Location</p> <p>This is a Contract to Hire position based out of Boston, Massachusetts.</p> <p>Pay and Benefits</p> <p>The pay range for this position is $84.00 - $96.00/hr.</p> <p>Eligibility requirements apply to some benefits and may depend on your job</p> <p>classification and length of employment. Benefits are subject to change and may be</p> <p>subject to specific elections, plan, or program terms. If eligible, the benefits</p> <p>available for this temporary role may include the following:</p> <ul> <li>Medical, dental & vision </li><li>Critical Illness, Accident, and Hospital </li><li>401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available </li><li>Life Insurance (Voluntary Life & AD&D for the employee and dependents) </li><li>Short and long-term disability </li><li>Health Spending Account (HSA) </li><li>Transportation benefits </li><li>Employee Assistance Program </li><li>Time Off/Leave (PTO, Vacation or Sick Leave) </li></ul> <p>Workplace Type</p> <p>This is a fully remote position.</p> <p>Application Deadline</p> <p>This position is anticipated to close on Aug 29, 2025.</p> <p>About Actalent</p> <p>Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.</p> <p>The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.</p> <p>If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.</p>