Quality Intern

Acadia Pharmaceuticals Inc.•Princeton, NJ

2d•$22 - $22•Hybrid

About The Position

Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson’s disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer’s disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we’re here to be their difference. The Quality intern will join the Quality Risk and Compliance team and collaborate with Quality and Research & Development partners to support improvements in clinical study quality oversight. Through exposure to study processes and performance metrics, the role will help enhance visibility, clarity, and effective monitoring of clinical study execution. This role is designed to provide meaningful, hands-on experience in a professional pharmaceutical environment, offering exposure to cross-functional collaboration, business processes, and industry best practices. Learn more about our internship program here.

Requirements

Currently enrolled in an accredited college or university pursuing a Bachelor’s degree in Life Sciences, Health Sciences, Engineering, Business, Data Analytics, or related disciplines.
Coursework or experience related to process improvement, statistics, project management, or healthcare systems preferred.
Minimum GPA of 3.0 preferred.
Interest in process improvement, data analysis, quality, healthcare, life sciences, or related fields.
Ability to organize information, identify patterns, and clearly communicate findings in writing and presentations.
Comfortable using common workplace tools such as Microsoft Excel, PowerPoint, Word, and Visio (or similar programs).
Strong communication skills, attention to detail, and a willingness to ask questions and learn new concepts.
Strong analytical and problem-solving skills with the ability to interpret data and identify trends.
Strong organizational and time-management skills with the ability to manage multiple priorities.
High level of professionalism, discretion, and ability to maintain confidentiality.
Ability to work both independently and collaboratively in a team-based environment.
Demonstrated initiative, curiosity, and willingness to learn in a fast-paced environment.

Nice To Haves

Prior internship, leadership experience, campus involvement, or project-based work preferred.
Interest in the pharmaceutical and/or biotechnology industry strongly preferred.

Responsibilities

Support clinical study quality oversight.
Assist with data analysis and report findings (written and presentation).
Collaborate with other teams, working with processes, metrics, reports, monitoring.
Improve how clinical study performance is monitored and communicated to improve consistency and reduce duplication in how clinical study metrics are defined, applied, and reviewed across studies.
Participates in team meetings, planning sessions, and strategic discussions to gain exposure to business operations and contribute insights where appropriate.
Demonstrates professionalism, accountability, and alignment with company values in all interactions.
Completes a capstone project or final presentation summarizing internship contributions and key learnings

Benefits

Competitive base, bonus, new hire and ongoing equity packages
Medical, dental, and vision insurance
Employer-paid life, disability, business travel and EAP coverage
401(k) Plan with a fully vested company match 1:1 up to 5%
Employee Stock Purchase Plan with a 2-year purchase price lock-in
15+ vacation days
13 -15 paid holidays, including office closure between December 24th and January 1st
10 days of paid sick time
Paid parental leave benefit
Tuition assistance