Associate Director, Clinical Data Management

Socket.dev; Boston (MA); On-site; USD 150,000 - 200,000; Full time

Job summary

Socket.dev in Boston is seeking an Associate Director of Clinical Data Management to lead data management across multiple clinical development programs. You will partner with cross-functional teams to ensure high-quality, inspection-ready data and timely database locks.

The role involves overseeing CROs, vendors, data quality, and regulatory submissions, driving data strategy and standards across studies in rare disease therapy development.

Responsibilities

• Lead and oversee all clinical data management activities for assigned clinical trials from protocol development through database lock and study closeout.
• Develop and execute data management strategies that support program timelines, quality objectives, and regulatory submission readiness.
• This role will serve as a key cross-functional leader, partnering with Clinical Operations, Biostatistics, Statistical Programming, Medical Writing, Pharmacovigilance, Regulatory Affairs, and external vendors to deliver study objectives while maintaining compliance with regulatory requirements and industry standards.

Job description

Reporting to: Sr.Director, Clinical Data Management

Do you have the passion and commitment to join a group whose mission is to develop treatments that have a clear and profound impact on patients suffering from rare diseases? Does it excite you to be a part of a patient-focused company developing potential new treatments that could dramatically improve the lives of patients with limited to no current treatment options? If yes, we encourage you to share with us your aspirations and career goals.

X4 is focused on restoring healthy immune system function by developing novel therapeutics to treat chronic neutropenic disorders, including WHIM syndrome, a rare primary immunodeficiency. We are advancing a novel, late-stage clinical candidate, mavorixafor, that we believe has the potential to become a new standard of care for patients with these disorders. We know that developing innovative, new medicines is challenging, and we invite new colleagues who share our values and commitment to join us in achieving our mission.

This opportunity will …

Provide strategic and operational leadership for clinical data management activities across one or more clinical development programs. The Associate Director will oversee CRO partners and vendors, drive data quality and inspection readiness, support regulatory submissions, and ensure the timely delivery of high-quality clinical trial data.

This role will serve as a key cross-functional leader, partnering with Clinical Operations, Biostatistics, Statistical Programming, Medical Writing, Pharmacovigilance, Regulatory Affairs, and external vendors to deliver study objectives while maintaining compliance with regulatory requirements and industry standards.

Accountabilities and Responsibilities:

Clinical Data Management Leadership

• Lead and oversee all clinical data management activities for assigned clinical trials from protocol development through database lock and study closeout.
• Develop and execute data management strategies that support program timelines, quality objectives, and regulatory submission readiness.