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Clinical Ink

Provides eSource tools for clinical trials

Data Management Intern

Data & AnalyticsConfirmed live in the last 24 hours
Internship · Fall 2026Horsham, PA, USANo salary listedIn-person

About the Job

Requirements

  • A high school diploma or equivalent is required.
  • Candidates must be currently enrolled in a college or university and have a minimum GPA of 3.0.
  • An understanding of data programming is advantageous.
  • Candidates must have strong verbal and written communication skills.
  • Candidates must be able to work in a team environment and take direction.
  • Candidates must be able to think critically and apply problem-solving skills.
  • Candidates must be able to interact with personnel at all levels cross-functionally.
  • Candidates must have strong organizational and time-management skills.
  • Candidates must have strong computer skills, including Microsoft Word, Excel, and PowerPoint.
  • Candidates must demonstrate superior attention to detail.
  • Candidates must be dependable and self-motivated.

Responsibilities

  • Assist the Project Data Manager with creating and maintaining study documentation.
  • Participate in study and project team meetings as needed, including preparing meeting minutes.
  • Assist with preparing Data Management presentations and training sessions.
  • Assist with revising Data Management standard operating procedures and related documentation.
  • Assist with data mapping and creating data exports.
  • Assist with quality-control reviews.
  • Assist with data-cleaning tasks, including query management, manual data review, and reconciliation.
  • Assist with database-lock and archival tasks.
  • Ensure the quality and timely completion of all assigned tasks.

Desired Qualifications

  • Life Science majors, such as biology, anthropology, or chemistry, are preferred.

About the Company

Clinical Ink

Provides eSource tools for clinical trials

Clinical Ink provides digital tools for clinical trials, focusing on eSource solutions such as Direct Data Capture (DDC), electronic Clinical Outcome Assessments (eCOA), electronic Patient-Reported Outcomes (ePRO), and electronic Consent (eConsent). These tools work by digitizing data collection and patient interactions: DDC captures data directly from sources, eCOA and ePRO collect outcomes and patient input electronically, and eConsent manages informed consent digitally—often via a subscription-based platform with optional rapid-build timelines and virtual trial support. The company differentiates itself through an end-to-end, scalable digital suite that emphasizes patient-centric data capture and global reach, aiming to streamline trials more than traditional, paper-based or disjointed systems. Its goal is to improve the quality and efficiency of clinical trials by delivering integrated, compliant eSource solutions to pharmaceutical companies, CROs, and academic institutions.

Company size
201-500
Company stage
Early VC
Total funding
$15M
Headquarters
Winston-Salem, NC
Founded
2007

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