eSource Developer III

We're on a Mission to Advance Clinical Discovery Patients are our ultimate why, and pioneering technology for patient outcomes is our DNA. Join us to advance the life sciences industry with technology solutions that transform the clinical trial experience for patients and put our research clients on the path to making confident, better‑informed decisions, faster. Benefits Robust benefits (medical, dental, vision, financial) Unlimited vacation Education assistance Parental leave Location: Remote Job Description Clinical Ink is seeking an eSource Developer III to join our Study Operations team based remotely across the United States. The eSource Developer III will serve as a subject matter expert and design and build electronic source documents that align with protocol requirements, ensuring quality, consistency, and usability. This role partners with cross‑functional stakeholders, mentors other team members, and drives efficient, standards‑based workflows in a fast‑paced, quality controlled environment. Responsibilities Program and review logic throughout the build process to confirm that specifications and requirements are suitable for users’ needs. Create, modify, and maintain electronic source documents based on protocol specifications or provided requirements. Review, recommend, implement, and utilize coding standards to maintain consistent workflow across the team. Reference protocol and/or other documentation to ensure expectations are met. Train and mentor new eSource Development team members, tracking training progress, teaching product functionality, use, and design, and shadowing new members on new study builds. Apply version control specifications to maintain document integrity and historical data. Communicate with other teams to ensure consistency within and across studies. Maintain client requests and updates in a fast‑paced, quality‑checked environment. Create printable paper source forms for user convenience, as needed. Provide technical assistance with problem solving for tickets. Work with Project Management and Study Build in drafting, reviewing, approving, and updating applicable project build and change control timelines. Other duties as assigned. Qualifications Bachelor’s degree in Computer Science or equivalent work experience. At least five years in a full‑time programming role. Ability to conceptualize large study builds and anticipate programming/coding challenges. Ability to organize, instruct and supervise staff, while promoting group effort in a matrix environment. Working knowledge of one or more Agile methodologies (i.e., TDD, SCRUM, or R‑SCRUM). Ability to identify needs and issues, track progress, and follow through on actions to meet customer satisfaction. Ability to communicate needs, issues, impacts, and corrective actions to varying levels of corporate personnel and customer leadership personnel. Demonstrated ability to manage conflicts and resolve problems effectively. Excellent written, verbal, and interpersonal communication skills; organizational skills and great attention to detail are required. Knowledge of complex scientific/office procedures and techniques relating to clinical research and patient care to accurately design source documents used to conduct clinical trials (preferred). Equal Employment Opportunity Clinical Ink is an equal opportunity employer and does not discriminate against otherwise qualified applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or handicap, or veteran status. #J-18808-Ljbffr Clinical Ink.