Regulatory Affairs Intern
Overview:
Undergraduate or Graduate student in a science discipline. This individual will work in our Regulatory Affairs Department, supporting the Regulatory Strategy group. He/she will be assigned interesting and challenging projects related to competitive data research, precedent analysis, regulatory environment monitoring and ad hoc projects. Additionally, the intern will have an opportunity to learn from and work with other functions within Product Development, such as Pharmacovigilance, Clinical Development and Medical Affairs to work on ad hoc projects and understand the roles of these functions within pharmaceutical industry. For this internship opportunity, we are looking for a bright, curious individual, with excellent work ethic, strong attention to detail and a passion to learn about the industry. Ideally, the candidate will have a strong interest in learning about Regulatory Affairs or is, perhaps contemplating a career in Regulatory Affairs within the pharmaceutical industry. Effective written and oral communication skills are important, along with the ability to interact successfully with your supervisor and associates in varied areas of expertise. This will be a rewarding internship experience and great learning opportunity. Along with your curriculum vitae, please also provide your responses to the Intern Program (IP) application questions. You must be available for the entire internship period (summer; no more than 90 days) and not have conflicting commitments (i.e., rotations, other employment) during that time. This internship will be primarily virtual with remote working and possible in-office attendance on an ad hoc basis depending on intern location. Relocation and housing costs will not be reimbursed.
Apply Now
Undergraduate or Graduate student in a science discipline. This individual will work in our Regulatory Affairs Department, supporting the Regulatory Strategy group. He/she will be assigned interesting and challenging projects related to competitive data research, precedent analysis, regulatory environment monitoring and ad hoc projects. Additionally, the intern will have an opportunity to learn from and work with other functions within Product Development, such as Pharmacovigilance, Clinical Development and Medical Affairs to work on ad hoc projects and understand the roles of these functions within pharmaceutical industry. For this internship opportunity, we are looking for a bright, curious individual, with excellent work ethic, strong attention to detail and a passion to learn about the industry. Ideally, the candidate will have a strong interest in learning about Regulatory Affairs or is, perhaps contemplating a career in Regulatory Affairs within the pharmaceutical industry. Effective written and oral communication skills are important, along with the ability to interact successfully with your supervisor and associates in varied areas of expertise. This will be a rewarding internship experience and great learning opportunity. Along with your curriculum vitae, please also provide your responses to the Intern Program (IP) application questions. You must be available for the entire internship period (summer; no more than 90 days) and not have conflicting commitments (i.e., rotations, other employment) during that time. This internship will be primarily virtual with remote working and possible in-office attendance on an ad hoc basis depending on intern location. Relocation and housing costs will not be reimbursed.
Apply Now