Oferta de trabajo: 2025 Summer Internship - Regulatory Affairs Clinical

The intern will work alongside experienced professionals, gaining insight into regulatory compliance and clinical study oversight.

Key Responsibilities:

• Support project management, including tracking action items and project milestones.

• Assist with the management of databases related to project strategies, clinical studies, and investigator audits.

• Contribute to authoring regulatory submissions, including meeting requests, controlled correspondence, and PADERs (Periodic Adverse Drug Experience Reports).

• Assist in the organization and tracking of clinical study documentation.

• Collaborate with teams to ensure regulatory compliance and data accuracy.

Qualifications & Skills:

• Currently pursuing a degree in Clinical Research, Regulatory Affairs, Pharmaceutical Sciences, or Chemistry.

• Completed coursework related to the areas of study above.

• Proficiency in Microsoft Office Suite.

• Strong computer skills, including database management.

• Excellent communication, teamwork, and organizational skills.

Benefits of the Internship:

• Gain hands-on experience in regulatory affairs and clinical research.

• Work alongside industry professionals and expand your professional network.

• Develop skills in regulatory compliance, project management, and clinical documentation.