eCOA Project Manager
Denmark, SC · On-site
Medable's mission is to get effective therapies to patients faster. We provide an end-to-end, cloud-based platform with a flexible suite of tools that allows patients, healthcare providers, clinical ...
eCOA Project Manager
Denmark, SC · On-site
Medable's mission is to get effective therapies to patients faster. We provide an end-to-end, cloud-based platform with a flexible suite of tools that allows patients, healthcare providers, clinical ...
Medable's mission is to get effective therapies to patients faster. We provide an end-to-end, agentic clinical trial platform with a flexible suite of tools that allows patients, healthcare providers ...
Medable's mission is to get effective therapies to patients faster. We provide an end-to-end, agentic clinical trial platform with a flexible suite of tools that allows patients, healthcare providers ...
Medable's mission is to get effective therapies to patients faster. We provide an end-to-end, agentic clinical trial platform with a flexible suite of tools that allows patients, healthcare providers ...
Medable's mission is to get effective therapies to patients faster. We provide an end-to-end, agentic clinical trial platform with a flexible suite of tools that allows patients, healthcare providers ...
Medable information
What is Medable?
Medable is a technology company that provides a cloud-based platform designed to streamline clinical trials and accelerate the development of new therapies. Their platform enables decentralized clinical trials, allowing for remote patient participation, real-time data collection, and improved patient engagement. By leveraging digital tools, Medable helps pharmaceutical companies, clinical research organizations, and healthcare providers reduce trial costs, increase efficiency, and improve patient access to cutting-edge treatments.
What are some common challenges Medable employees face when working on decentralized clinical trial projects?
Medable team members often navigate the complexities of coordinating clinical trials that span multiple sites and use digital tools for patient engagement and data collection. Challenges include ensuring seamless communication among cross-functional teams, adapting to rapidly evolving regulatory requirements, and maintaining data integrity in a remote environment. However, Medable’s collaborative culture and emphasis on continual learning help employees address these challenges while advancing innovation in clinical research.
What are the key skills and qualifications needed to thrive as a Clinical Trial Project Manager at Medable, and why are they important?
To excel as a Clinical Trial Project Manager at Medable, you need a solid background in clinical research, project management, and a relevant life sciences degree. Familiarity with electronic data capture (EDC) platforms, Medable's decentralized clinical trial technology, and regulatory compliance systems is crucial. Strong leadership, organizational skills, and effective communication help in managing teams and stakeholder expectations. These skills are vital for successfully delivering clinical studies on time, ensuring regulatory adherence, and maintaining high-quality patient outcomes.
What is the difference between Medable vs Clinical Research Coordinator?
| Aspect | Medable | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Typically requires a background in healthcare, clinical research, or related fields; certifications like CCRP are common | Often requires a bachelor's degree in health sciences or related field; certifications like CCRP or CRC preferred |
| Work Environment | Primarily remote or hybrid; utilizes digital platforms for decentralized clinical trials | Usually onsite at research sites or hospitals; involves direct interaction with patients and staff |
| Employer & Industry Usage | Used by biotech, pharma, and clinical research organizations focusing on decentralized trials | Employed by hospitals, research institutions, and CROs conducting traditional clinical studies |
Medable and Clinical Research Coordinators both operate within the clinical research industry, but Medable focuses on digital, decentralized trial platforms often enabling remote work, while Clinical Research Coordinators typically work onsite managing traditional clinical studies. The roles share similar credentials but differ mainly in work environment and technological focus.
More about Medable jobs
What states have the most Medable jobs?
States with the most job openings for Medable jobs include:
What job categories do people searching Medable jobs look for?
The top searched job categories for Medable jobs are:
eCOA Project Manager
Denmark, SC • On-site
Medable, Inc.
• Software Development • 501 - 1,000 employees501 - 1,000 employees
Full-time
Posted 18 days ago
Job description
Medable's mission is to get effective therapies to patients faster. We provide an end-to-end, cloud-based platform with a flexible suite of tools that allows patients, healthcare providers, clinical research organizations and pharmaceutical sponsors to work together as a team in clinical trials. Our solutions enable more efficient clinical research, more effective healthcare delivery, and more accurate precision and predictive medicine. Our target audiences are patients, providers, principal investigators, and innovators who work in healthcare and life sciences.
Our vision is to accelerate the path to human discovery and medical cures. We are passionate about driving innovation and empowering consumers. We are proactive, collaborative, self-motivated learners, committed, bold and tenacious. We are dedicated to making this world a healthier place.
Responsibilities- Manage the initial deployment lifecycle of the Medable Solution spanning project kick-off through go-live and system localization.
- Collaborate with solution design teams to ensure a comprehensive understanding of trial-specific requirements.
- Manages project scope, timelines and financial oversight, including submitting and approving timecards (as applicable) and ensuring the project remains within budget.
- Ensure the design teams align the System Specifications to the clinical trial protocols and detailed schedules of assessments within the scope of the study contract
- Develop adaptive project plans seamlessly incorporating evolving client needs and trial requirements without disrupting project momentum.
- Implement robust change management practices by proactively identifying, evaluating, and integrating change requests.
- Educate clients and internal teams on software capabilities, customization options, and best practices for integration into clinical trial processes.
- Provide expert oversight for ongoing projects requiring system enhancements or modifications.
- Take decisive action to realign project deliverables when requirements or priorities shift.
- Ensure continuous progress and maintain project integrity.
- Facilitate the translation of client requirements into fully functional software solutions.
- Develop and execute comprehensive, detailed project plans
that strategically outline timelines, critical milestones, and optimal resource allocation. - Support successful software implementation through coordinated planning and execution.
- Build and maintain strong, collaborative relationships with clients through transparent and consistent communication serving as the primary point of contact for all project updates, issue resolution, and ongoing support.
- Proactively identify potential risks and challenges throughout the project lifecycle.
- Develop strategic mitigation strategies that anticipate potential obstacles.
- Create comprehensive guidance materials and conduct knowledge transfer sessions for the Study Conduct team.
- Collaborate extensively with cross-functional teams including developers, product managers, and clinical trial experts.
- Facilitate cohesive communication to ensure delivery of solutions that meet complex client and regulatory expectations.
- Conduct rigorous analysis of project outcomes to identify opportunities for methodological refinement and process improvement.
- Drive continuous organizational enhancement through data-driven insights and recommendations.
- Other duties as assigned.
- Minimum of 6 years of experience or an equivalent combination of related education and experience.
- Proven experience in managing full lifecycle software implementation projects with a track record of supporting solution design and delivery tailored to specific client requirements.
- Advanced proficiency in change management showcasing the ability to handle complex change requests and effectively coordinate cross-functional teams with updated project objectives.
- Extensive experience supporting in-flight projects requiring adaptive approaches or enhanced oversight.
- Comprehensive understanding of clinical trial domains, specifically:
- eCOA (electronic Clinical Outcome Assessments)
- ePRO
- EDC
- DCT
- Strong knowledge of clinical trial data management processes and regulatory compliance frameworks.
- Exceptional project management capabilities, including:
- Supporting development of detailed, strategic project plans.
- Managing multiple complex priorities simultaneously.
- Maintaining high-quality standards under dynamic conditions.
- Outstanding interpersonal, leadership, and communication skills with demonstrated ability to communicate effectively in both oral and written formats.
- Technical aptitude with rapid learning capability and ability to effectively coordinate utilization of diverse software tools.
- Bachelor's degree in Computer Science, Health Informatics, or related field.
- Master's degree in Computer Science, Health Informatics, or relevant domain (preferred).
- Project Management Professional (PMP), PRINCE2, or other equivalent project management certifications.
- Flexible travel schedule to meet project and client needs potentially involving domestic and international destinations.
At Medable, we believe that our team of Medaballers is our greatest asset. That is why we are committed to your personal and professional well-being. Our rewards are more than just benefits - they demonstrate our commitment to providing an inclusive, healthy and rewarding experience for all our team members.
Flexible Work
Remote from the start, we believe in a flexible employee experience
Compensation
Competitive base salaries
Annual performance-based bonus
Stock options for employees, aligning personal achievements to Medable's success
Health and Wellness
Health and insurance coverage
Wellness program (Mental, Physical and Financial)
Recognition
Peer-to-peer recognition program, celebrating achievements and milestones
Community Involvement
Volunteer time off to support causes you care about
Medable is committed to providing reasonable accommodations for qualified individuals with disabilities in our job application procedures. If you need assistance or would like to request an accommodation due to a disability, please contact us athr@medable.com.
About Medable
Sourced by ZipRecruiter
Industry
Software development
Company size
501 - 1,000 Employees
Headquarters location
Palo Alto, CA, US
Year founded
2016