Project Coordinator

Posted 7 Days Ago
Be an Early Applicant
Hiring Remotely in Costa Rica
Remote
Junior
Healthtech • Software
The Role
Coordinate eCOA study activities supporting project managers across planning, setup, monitoring, and close‑out. Assist with eCOA system configuration, device deployment/tracking, study documentation, reporting, meetings, and financial follow‑ups. Liaise with clients and cross‑functional teams, track and escalate issues, ensure training compliance, and contribute to process improvements to support efficient clinical trial execution and high‑quality patient‑reported data.
Summary Generated by Built In

At Clario, a part of Thermo Fisher Scientific, we are committed to transforming clinical trials through technology and innovation. As a Project Coordinator (eCOA), you will play a key role in supporting the successful delivery of clinical trials by partnering closely with Project Managers and cross‑functional teams. This role focuses on coordinating eCOA study activities, supporting digital data collection solutions, and ensuring high‑quality documentation throughout the study lifecycle. Your work will contribute to efficient study execution and the delivery of reliable patient‑reported data that advances clinical research and improves patient outcomes.

What We Offer

  • Competitive compensation
  • Comprehensive health and wellness benefits
  • Paid time off and company holidays
  • Engaging employee programs

What You’ll Be Doing

  • Support Project Management teams across all study phases, including planning, setup, monitoring, and close‑out
  • Assist with configuration and setup activities for eCOA systems and study databases
  • Support development, review, and maintenance of study documentation and system specifications
  • Coordinate deployment, tracking, and reconciliation of eCOA devices and/or digital data collection tools
  • Prepare, maintain, and distribute study reports, metrics, and documentation
  • Organize and support project meetings, including agendas, meeting minutes, and action item tracking
  • Support financial processes such as documentation updates for scope changes, invoice reconciliation follow‑ups, and forecasting reports
  • Ensure compliance with training requirements and proper documentation of completion
  • Respond to client inquiries and participate in client calls and meetings as requested
  • Support cross‑functional collaboration with teams such as Data Science, Software/IT, and Clinical Operations
  • Track, document, and escalate issues, ensuring timely resolution of system or study‑related risks
  • Contribute to process improvements and optimization of eCOA workflows and tools

What We Look For

  • 1–3+ years of experience in pharmaceutical, clinical research, or a related industry
  • Bachelor’s degree preferred with understanding of the drug development process
  • Familiarity with eCOA, eClinical technologies, or electronic data capture systems preferred
  • Strong organizational, time management, and prioritization skills
  • Excellent written and verbal communication skills in English
  • High attention to detail with a proactive and responsive mindset
  • Ability to work independently and collaboratively in a fast‑paced, global, matrixed environment
  • Proficiency with Microsoft Office applications
  • Strong interpersonal skills and ability to coordinate across cross‑functional teams
  • Adaptability to changing priorities and project needs

At Clario, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting global teams, your work helps bring life‑changing therapies to patients faster.

Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.

Skills Required

  • 1-3+ years of experience in pharmaceutical, clinical research, or a related industry
  • Bachelor's degree (preferred) with understanding of the drug development process
  • Familiarity with eCOA, eClinical technologies, or electronic data capture systems
  • Strong organizational, time management, and prioritization skills
  • Excellent written and verbal communication skills in English
  • High attention to detail with a proactive and responsive mindset
  • Ability to work independently and collaboratively in a fast-paced, global, matrixed environment
  • Proficiency with Microsoft Office applications
  • Strong interpersonal skills and ability to coordinate across cross-functional teams
  • Adaptability to changing priorities and project needs

Clario Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Clario and has not been reviewed or approved by Clario.

  • Leave & Time Off Breadth Time off is described as generous, including flexible PTO for some roles and up to 26–31 PTO days for eligible staff. The calendar includes 15 paid company holidays and a Winter Break.
  • Healthcare Strength Healthcare offerings include multiple medical plan options via Highmark with coordinated care navigation, plus dental and vision through established carriers. Employer HSA contributions and mental-health support broaden the package.
  • Inclusive Benefits Coverage Coverage highlights include domestic-partner eligibility, transgender-inclusive care, and HIV prevention/treatment. These inclusive elements are presented alongside broader inclusion commitments.

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The Company
HQ: Philadelphia, PA
6,733 Employees
Year Founded: 1972

What We Do

-- Clario has been named a Top Workplace by Energage for the 2022 Top Workplaces USA national awards. -- Clario generates the richest clinical evidence by fusing our deep scientific expertise and global scale into the broadest endpoint technology platform. By doing this, we empower our partners to transform lives. With almost 50 years of experience, 19,000 clinical trials, and 870 regulatory approvals, Clario has mastered the ability to generate rich evidence across a Trial Anywhere™ portfolio: decentralized (DCT), hybrid and site-based clinical trials. With 30 facilities in nine countries across North America, Europe, and Asia Pacific, Clario delivers the power of certainty. Partners ————— Clario brings the best of ERT and Bioclinica together to work alongside our partners to solve some of their biggest questions on topics such as: - eCOA vs. paper - Decentralized Clinical Trial (DCT) - Rescue a clinical trial - Broad endpoint technology: cardiac safety, imaging, respiratory And many more. People ———— We are so honoured to be named a 2022 Top Workplace by Energage. One of our leading values at Clario is People First Always. We help individuals build meaningful careers at Clario as they serve to help transform patients lives. Join us on this journey and check out our careers page: https://clario.com/careers/

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