Intern, Clinical Data Management at Eikon Therapeutics

Jersey City, New Jersey, United States -

Full Time

Start Date

Immediate

Expiry Date

26 May, 26

Salary

36.0

Posted On

25 Feb, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Veeva CDMS, Study Build, UAT, Data Review, Data Cleaning, Data Freeze, R, Python, SQL, Data Analysis, Attention To Detail, Organization, Problem-Solving, Communication, Collaboration

Industry

Biotechnology Research

Description

Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon’s discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets. Position This 10-week summer internship provides an opportunity to gain hands-on experience within the Clinical Data Management (CDM) function in a fast-paced, collaborative biotech environment. The Clinical Data Management Intern will support study start-up, study conduct, and data freeze activities across clinical development programs, with a strong focus on Veeva CDMS system activities and clinical data review. In this role, you will gain exposure to the end-to-end clinical data management lifecycle, including study build, user acceptance testing (UAT), data review, and clinical data delivery activities that support clinical trial execution and regulatory submissions. About You You are passionate about improving patient outcomes through high-quality clinical data and are interested in learning how clinical trial data is collected, reviewed, and prepared for analysis. You are detail-oriented, organized, and enjoy working with data while collaborating with cross-functional teams. You are a logical thinker who is curious, eager to learn, and excited to gain exposure to real-world clinical development processes in a dynamic environment. What You’ll Do Support Veeva CDMS study build activities. Assist with data management start-up activities, including preparation of study documents such as eCRF requirement documents, eCRF completion guidelines, integrated data review plans, and data quality management plans. Participate in User Acceptance Testing (UAT), including development and execution of test scripts. Assist with external data setup and validation testing. Support ongoing data review activities, including review of EDC queries, manual listings, and data quality checks. Assist with interim data cleaning and data freeze preparation and delivery. Support clinical data delivery activities, including block cleaning and study data deliverables. Contribute to programming and process improvement initiatives, including supporting automation of test scripts. Assist with quality control and validation of reports and dashboards. Present internship project outcomes and key learnings. Qualifications Currently enrolled in an accredited university pursuing a Bachelor’s degree in Computer Science, Engineering, Informatics, Biology, Chemistry, Pharmaceutical Sciences, or a related field. Completed at least two years of undergraduate coursework. Must be enrolled in school during the internship program. Programming experience with R or Python, SQL and related data analysis tools. Strong attention to detail and organizational skills. Strong analytical, problem-solving, verbal, and written communication skills. Ability to work collaboratively in a team environment. Comfort working with data and learning new systems. Must be available to work full-time (40 hours per week) during core business hours for a minimum of 10 weeks during the summer internship program. Completion of coursework in Data Science, Artificial Intelligence or related analytical disciplines preferred. The expected hourly pay rate for this role is $36/hour. Eikon is proud to be an equal opportunity employer and will consider all qualified applicants for employment. We are currently not accepting any new third-party agencies or firms at this time. Please do not forward unsolicited agency resumes to our website, employees or Human Resources. Eikon Therapeutics will not pay fees to any third-party agency or firm associated with unsolicited resumes.

Responsibilities

The intern will support study start-up, conduct, and data freeze activities across clinical development programs, focusing heavily on Veeva CDMS system tasks and clinical data review. Responsibilities include assisting with study build, User Acceptance Testing (UAT), external data setup, ongoing data quality checks, and supporting data delivery activities.