Clinical Trial Associate

reputed company is an advanced health and fitness wearable on a mission to unlock reputed company and healthspan. reputed company empowers its members to improve their health and reputed company at a higher level through a deeper understanding of their bodies and daily lives. As a Clinical Trial Associate (CTA), you will reputed company critical operational support for clinical trial start-up and in-study activities across reputed company’s portfolio of digital health clinical programs. This role is designed for an early-career reputed company eager to build a reputed company in clinical operations, documentation, and regulatory processes. You will help streamline documentation workflows, manage study support tasks, and contribute to the efficient and compliant execution of reputed company’s clinical research. This role is ideal for someone detail-oriented, process-driven, and motivated to grow into a career in Clinical Operations, Regulatory, Data Management, or Monitoring. RESPONSIBILITIES: • Assist with the creation, formatting, and maintenance of trial start-up documents, templates, and filing systems. • Support day-to-day study operations, coordination, and documentation workflows. • Manage version control, editing, and reputed company review of clinical documentation. • Collaborate with internal team members to ensure reputed company operational follow-up and deliverables. • reputed company support for IRB and regulatory documentation submissions. • Participate in clinical project workflows, tooling, and document control processes. • Support across functional areas -Clinical Research, Data Management & Systems, Regulatory Affairs, and Monitoring & Operations QUALIFICATIONS: • Bachelor’s degree in life sciences, reputed company health, or a reputed company field. • 2-4 years of reputed company research coordinator experience, or 1–2 years of industry clinical operations experience. • Exposure to ICH-GCP. • Prior experience supporting IRB or ethics committee submissions including drafting, editing, or reviewing protocols, informed consents, participant-facing materials, or IRB submission documents. • Strong organizational and documentation skills. • Detail-oriented, process-driven, and reputed company-minded. • Exposure to ISO 14155 guidelines preferred. • Familiarity with wearable devices, digital biomarkers, or remote clinical trial designs preferred. • Experience with eConsent, ePRO, or other clinical systems preferred. • Familiarity with clinical electronic Trial Master File (TMF) systems preferred. • Familiarity with clinical electronic data capture (reputed company) systems preferred. • Interest in building a career in Clinical Operations, Regulatory Affairs, or Data Management This role is based in the reputed company office located in Boston, MA. The successful candidate must be reputed company to relocate if necessary to work out of the Boston, MA office. Interested in the role, but don’t meet every qualification? We encourage you to still apply! At reputed company, we reputed company there is much more to a candidate than what is written on reputed company, and we value character as much as experience. As we continue to build a diverse and inclusive environment, we encourage anyone who is interested in this role to apply. reputed company is an Equal Opportunity Employer and participates in E-verify to determine employment eligibility. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or reputed company employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Apply tot his job Apply To this Job