Global Clinical Trial Manager - Lead High-Impact Trials

Disc Medicine; New York (NY); On-site; USD 150,000 - 190,000; Full time

Job summary

Disc Medicine seeks a Senior Clinical Trial Manager to lead the planning, execution, and closeout of large global clinical trials. The role involves managing CROs and vendors, maintaining regulatory compliance, and collaborating with cross-functional teams in a fast-paced biopharmaceutical environment.

Responsibilities include overseeing trial closeouts, selecting CROs, drafting essential documents, ensuring GCP audit readiness, and monitoring budgets and timelines across global studies.

Qualifications

• Bachelor's degree in any discipline.
• 7+ years of clinical trial management experience.
• Experience with global study management and GCP regulatory requirements.
• Strong written and oral communication skills.
• Experience managing CROs and external vendors.

Responsibilities

• Plan, execute, and oversee the closeout of global clinical trials.
• Evaluate, select, and manage CROs and external vendors.
• Write and review protocols, informed consent forms, and regulatory reports.
• Ensure trial master files meet GCP standards and audit readiness.
• Monitor progress, budgets, timelines, and identify risks.

Skills

Global study management

CRO management

Vendor management

GCP/regulatory knowledge

Communication skills

Education

Bachelor's degree in any discipline

Job description

Disc Medicine seeks a Senior Clinical Trial Manager to lead the planning, execution, and closeout of large global clinical trials. The role involves managing CROs and vendors, maintaining regulatory compliance, and collaborating with cross-functional teams in a fast-paced biopharmaceutical environment.

Responsibilities include overseeing trial closeouts, selecting CROs, drafting essential documents, ensuring GCP audit readiness, and monitoring budgets and timelines across global studies.