Regulatory Compliance Coordinator: Clinical Trials Disclosures

Integrated Resources Inc.; Woodcliff Lake (NJ); On-site; USD 80,000 - 100,000; Full time

Benefits offered by this job

Referral bonus

Job summary

A leading staffing firm seeks a Regulatory Affairs professional to coordinate clinical disclosure activities. The role demands expertise in clinical trial transparency principles and at least 3 years of experience in pharmaceutical R&D. Responsibilities include ensuring compliance with global regulations and maintaining strong internal relationships.

Qualifications

• At least 3 years working in the pharmaceutical industry in an R&D environment.
• Solid knowledge of clinical trial transparency principles, preferably on an international level.
• Ability to work as part of a team across multiple departments.

Responsibilities

• Coordinating the posting of registration and disclosures on clinicaltrials.gov and EudraCT.
• Ensuring trial disclosure compliance with applicable regulations globally.
• Maintaining disclosure trackers and producing metrics reports for management.

Skills

Attention to detail

Communication skills

Influencing skills

Job description

A leading staffing firm seeks a Regulatory Affairs professional to coordinate clinical disclosure activities. The role demands expertise in clinical trial transparency principles and at least 3 years of experience in pharmaceutical R&D. Responsibilities include ensuring compliance with global regulations and maintaining strong internal relationships.