Summer Internship - Clinical Research & Development

Hikma Pharmaceuticals USA Inc. • Columbus, OH

3d • $19 • Onsite

About The Position

As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates’ purpose is to put better health within reach, every day for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 760 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high-quality medicines accessible to the people who need them.
We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated College Summer Intern for our Clinical Resarch and Development team at our Columbus, Ohio site. As an Intern, you will earn practical experience as a fully integrated member of our team and participate in meaningful projects that will add value to our organization. In this role, you will provide support to the various Research and Development groups, Participate in Clinical Research Trial Design and Implementation.

Requirements

• Regular and predictable onsite attendance and punctuality.
• Must be an Undergraduate, Graduate, or Professional Student in good academic standing.
• Must have completed 12 credit hours within a related major and/or other related coursework.
• Overall, cumulative GPA must be at least 3.0 (on 4.0 scale) or better.
• Pursuing degree in a scientific discipline.
• Must be able to demonstrate effective communication skills.
• Strong mathematical, analytical, and problem-solving abilities.
• Highly motivated and inquisitive with a strong desire to learn.
• Organization skills to manage multiple tasks with strong attention to details.
• Proficiency in Microsoft Office applications (Excel, Word, PowerPoint required; data analysis experience a plus).
• Strong verbal and written communication skills, with the ability to communicate clearly with cross-functional teams.
• Demonstrated initiative, positive attitude, and willingness to learn and support the Materials Management team.
• Ability to wear required personal protective equipment (PPE) and work in an operational environment as needed.
• Must be legally authorized to work in the United States without restriction; no sponsorship offered at this time.
• Must be willing to submit to a background investigation, including verification of employment, criminal history, and educational background.
• Must be willing to take a drug test.
• Must be 18 years of age or older.

Responsibilities

• Learn to conduct Clinical Trials developing experience in Phase I-IV, Bioequivalence, and Biosimilar studies/ Review and Learn Good Clinical Practice.
• Review and Learn Good Manufacturing Practice.
• Participate in Regulatory Filings to support ANDA and IND submissions to FDA, Health Canada, and other regulatory agencies.
• Develop a working knowledge of Standard Operating Procedures (SOP’s).
• Facilitate writing technical documents and presentations.
• Learn regulations for FDA Guidance, DEA Requirements, ICH Ethical Standards.
• Gain Project Management Experience.

What This Job Offers

• Career Level: Intern
• Education Level: No Education Listed
• Number of Employees: 5,001-10,000 employees