Clinical Affairs Intern (CAI)

Job Description

About Company

• Lensa: Lensa is a career site dedicated to helping job seekers find employment in the US. It is not a staffing firm or agency and does not directly hire for the jobs it lists. Instead, Lensa promotes job opportunities on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. For this specific job, Lensa partners with DirectEmployers to promote a position for Zimmer Biomet. When users click “Apply Now” or “Read more” on Lensa, they are redirected to the job board or employer’s own site, where any information collected is subject to their respective terms and privacy notices.

• Zimmer Biomet: Zimmer Biomet is a global medical technology leader with nearly 100 years of history. The company’s core mission involves pushing the boundaries of innovation to enhance patient mobility and restore lives. A Zimmer Biomet product or technology contributes to enhancing a patient’s mobility every 8 seconds. The company is committed to its team members, focusing on providing development opportunities, robust employee resource groups (ERGs), a flexible working environment, location-specific competitive total rewards, wellness incentives, and a culture that emphasizes recognition and performance awards. Zimmer Biomet strives to create an inclusive environment where every team member feels respected, empowered, and recognized.

Job Description: Clinical Affairs Intern (CAI)

• Job Title: Clinical Affairs Intern (CAI)

• Reporting Structure: The Clinical Affairs Intern operates under the direct supervision of a Clinical Project Manager.

• Job Summary: This role is primarily responsible for performing administrative activities that support ongoing MDR (Medical Device Regulation) and Clinical projects. These projects span various business units including hip, knees, sport medicine, trauma, and extremities. The position requires a basic understanding of the medical device industry, regulatory concepts, product lifecycle data, and project management principles.

• Key Responsibilities (What You Can Expect / How You’ll Create Impact):
• Manage scope traceability for files that fall under MDR regulations.
• Collaborate with multiple stakeholders to define objectives, timelines, and milestones specifically within the Medical Writing and Post Market Surveillance (PMS) Department.
• Participate in project teams, which includes attending meetings and presentations.
• Support team members by ensuring proper tracking of project activities.
• Report out to Leadership on the current status of projects, identifying issues, and proposing mitigations.

• Required Skills & Competencies (What Makes You Stand Out):
• Basic computer skills, including proficiency in Microsoft Office Suite.
• Strong writing and communication skills.
• Strong interpersonal skills.
• Strong Analytical Skills with a keen affinity for details.
• Versatility, flexibility, and a willingness to adapt to changing priorities.
• Strong organizational, teamwork, problem-solving, and analytical skills are essential.
• Ability to work autonomously and efficiently on specific tasks.
• Ability to work with rapid changes.
• Ability to learn regulations pertinent to medical devices.
• Ability to learn basics of medical device regulations.
• Ability to handle multiple projects and meet deadlines, working closely with RA Specialists and Managers.

• Educational Background (Your Background):
• Must be actively enrolled in an academic program for the entire duration of the assignment.
• Candidates should be pursuing a Bachelor’s Degree in health, life sciences, or engineering disciplines.
• A GPA of 3.0 or higher is strongly preferred.

• Travel Expectations: The role may require up to 5% travel.

• Diversity & Inclusion: Zimmer Biomet is an EOE/M/F/Vet/Disability employer, committed to equal opportunity.

• Contact for Questions: For any inquiries regarding this job posting, please contact support@lensa.com.