Clinical Trial Co-op Associate, Immunoassay, Clinical Program Strategy

Why Sarepta? Why Now?

The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more than 40 programs in various stages of development in gene therapy, RNA and gene editing. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne.
 

We’re looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients.
 

What Sarepta Offers

At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity.

The Importance of the Role
 

The Clinical Trial Co-op will report into the Clinical Operations Program Lead (COPL), Immunoassay, Clinical Program Strategy and is responsible for the assessment, development, and improvement of clinical operational processes and supportive tools. As a co-op, you will gain valuable hands-on experience working alongside the Clinical Operations Program Lead on real-world projects, including process improvement initiatives, while learning about our clinical trial operating model.

The Opportunity to Make a Difference

This application is for a 6-month co-op program that will start on July 7th, 2025, and conclude on December 19th, 2025. This is a full-time, 40 hours a week, co-op program.

• Perform gap analysis of Sarepta’s processes and procedures against medical device diagnostics.

• Apply learnings from gap assessment to applicable processes and procedures.

• Conduct impact assessment on other initiatives related to integration of medical device diagnostics and support process improvement activities as required.

• May support additional ad-hoc activities as agreed with the manager.

• Share lessons learned and key takeaways with Development Operations at regular meetings and during a final presentation forum.

More about You

• Undergraduate (junior or senior) or graduate student pursuing a degree in Biotechnology, Regulatory, Business, Public Health, Healthcare Administration, Clinical Research, Biology, or Biomedical Sciences.

• Remote, however, opportunities to go on-site to Cambridge, MA office for face-to-face meetings

• Desire to work in a dynamic, fast-paced team environment and make a difference in the lives of patients

• A motivated team player that values learning and working in a team environment

• Strong computer skills including knowledge of Excel, Work, PowerPoint and Outlook

• Solid interpersonal skills and solid organizational skills

• Solid written and verbal communication skills

• Knowledge of regulatory requirements and clinical trial conduct

What Now?

We’re always looking for solution-oriented, critical thinkers.

So, if you’re comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply.
 

#LI-Remote#LI-MC1

This position is remote. However, you will be expected to work on site at one of Sarepta's facilities in the United States and/or attend Company-sponsored in-person events from time to time.

The targeted salary range for this position is $22 - $34 per hour depending upon years of education completed and nature of role.

Candidates must be authorized to work in the U.S.

Sarepta Therapeutics offers a competitive compensation and benefit package.

Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify. Apply