Regulatory Portfolio Management Intern
Welcome to Bristol-Myers Squibb, a global biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines to patients in need. We are seeking a highly motivated and detail-oriented individual to join our team as a Regulatory Portfolio Management Intern. This is a unique opportunity to gain hands-on experience in the ever-evolving field of regulatory affairs and contribute to the success of our company. If you are a self-starter with a passion for the healthcare industry and a strong desire to learn and grow, we encourage you to apply.
- Conduct research and analysis of regulatory guidelines and requirements for various markets.
- Assist in the preparation and submission of regulatory documents to health authorities.
- Maintain and update regulatory databases and tracking systems.
- Collaborate with cross-functional teams to ensure timely and accurate completion of regulatory submissions.
- Support the development and maintenance of regulatory processes and procedures.
- Attend and participate in team meetings and provide updates on project progress.
- Communicate with internal and external stakeholders regarding regulatory matters.
- Review and provide input on labeling and packaging materials for compliance with regulatory requirements.
- Assist in the preparation of regulatory reports and presentations.
- Stay up-to-date with industry trends and changes in regulatory landscape.
- Adhere to company policies and regulatory guidelines.
- Complete assigned projects and tasks within specified timelines.
- Maintain confidentiality of sensitive information.
- Participate in training and development opportunities to enhance knowledge and skills.
- Demonstrate a strong work ethic, attention to detail, and a positive attitude.
Strong Understanding Of Regulatory Affairs: The Ideal Candidate For A Regulatory Portfolio Management Intern At Bristol-Myers Squibb Should Have A Solid Understanding Of The Regulatory Landscape And Processes Involved In Drug Development.
Excellent Analytical And Problem-Solving Skills: As A Regulatory Portfolio Management Intern, The Candidate Will Be Responsible For Analyzing Complex Data And Identifying Potential Issues, So Strong Analytical And Problem-Solving Skills Are A Must.
Attention To Detail: The Pharmaceutical Industry Is Highly Regulated, And Even A Small Error In Regulatory Submissions Can Have Significant Consequences. Therefore, Attention To Detail Is A Critical Qualification For This Role.
Familiarity With Project Management Principles: The Regulatory Portfolio Management Intern Will Be Involved In Managing Various Projects Related To Regulatory Submissions. Therefore, Familiarity With Project Management Principles And Tools Is Essential For Success In This Role.
Strong Communication Skills: The Ability To Effectively Communicate Complex Regulatory Information To Diverse Stakeholders, Including Cross-Functional Teams And Regulatory Agencies, Is Crucial For A Regulatory Portfolio Management Intern At Bristol-Myers Squibb.
Process Improvement
Communication Skills
Project Management
Data Analysis
Time Management
Attention to detail
Quality Control
Research skills
Compliance Management
Teamwork
Regulatory Affairs
Risk
Communication
Conflict Resolution
Leadership
Time management
Interpersonal Skills
creativity
Teamwork
Adaptability
Problem-Solving
Decision-making
According to JobzMall, the average salary range for a Regulatory Portfolio Management Intern in Redwood City, CA, USA is between $20 and $30 per hour, with a median hourly rate of $25. This equates to an annual salary range of approximately $41,600 to $62,400. However, this can vary depending on factors such as the specific company, the intern's level of experience, and the responsibilities and tasks assigned to them during their internship.
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Bristol-Myers Squibb Co. operates as a biopharmaceutical company, which engages in the discovery, development, licensing, manufacturing, marketing, distribution, and sale of biopharmaceutical products. It includes chemically-synthesized drugs or small molecules and products produced from biological processes called biologics.
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