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Last Name*

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Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

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Are you an employer or a jobseeker?*

Message

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Job type: Permanent

Discipline: Project Manager, Publishing & Submissions, RA Intelligence

Location: United States

Proclinical is currently recruiting for a Regulatory Affairs Analyst with a biopharmaceutical company located in North Chicago, IL.

Job Responsibilities:

Reviews, and assess' incoming global regulatory information for entry into registration and documentation management systems.
Interacts with all areas of regulatory affairs and affiliates to ensure registration management information is current, accurate and available in regulatory systems.
Executes established business processes and may assist in development and implementation of process/system changes and/or data remediation projects.
Troubleshoots errors and system performance issues and works with supervisor and IT on business problem resolution and enhancements.
Participates and contributes to group, department, and cross-functional meetings.
May also assist in training junior team members.

Skills and Requirements:

Bachelor's Degree, 4+ years in a related area including manufacturing, regulatory affairs, R&D, or quality in the pharmaceutical, medical device, or other healthcare industry.
Experience/understanding/use of software tools.
Demonstrated analytical and communication skills.
Skills and knowledge of drug submissions

If you are having difficulty in applying or if you have any questions, please contact Samantha Reader at 267-536-3075.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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