Clinical Trials Regulatory Specialist

Weill Cornell Medicine - Qatar; New York (NY); On-site; USD 70,000 - 90,000; Full time

Job summary

Weill Cornell Medicine - Qatar seeks a regulatory specialist to oversee the regulatory maintenance of clinical trials from submission through closeout. You will coordinate protocol submissions to the CSEC, IRB, and ancillary committees, ensuring all regulatory documents are accurate and current to support enrollment and study conduct.

The role requires a Bachelor’s degree in a related field and ~2 years of clinical research experience in healthcare.

Qualifications

• Bachelor's Degree in related field required.
• Approximately 2 years of clinical research experience in healthcare.
• CCRP preferred; Master’s degree may substitute for experience.

Responsibilities

• Oversees regulatory maintenance for clinical trials from submission to closeout.
• Coordinates protocol submissions to the CSEC, IRB, and ancillary committees.
• Ensures regulatory compliance and up-to-date records; submits regulatory documents to sponsors/CROs.

Skills

Communication skills

Interpersonal skills

MS Office

Detail orientation

Multitasking

Collaboration

Discretion

Professionalism

Education

Bachelor's Degree in related field

Master’s degree substitution for experience

Tools

MS Office Suite

Database applications

Job description

Weill Cornell Medicine - Qatar seeks a regulatory specialist to oversee the regulatory maintenance of clinical trials from submission through closeout. You will coordinate protocol submissions to the CSEC, IRB, and ancillary committees, ensuring all regulatory documents are accurate and current to support enrollment and study conduct.

The role requires a Bachelor’s degree in a related field and ~2 years of clinical research experience in healthcare.