Jobs and Careers
WO

eCOA Manager, Clinical Assessment Technologies Operations

Worldwide Clinical Trials
Virtual United States North Carolina, United States, United StatesRemotefull_timeVerifiedPosted 24 Sept 2025

About the role

Who we are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!

What Clinical Assessment Technologies Department does at Worldwide

Clinical Assessment Technologies (CAT) is a team of highly experienced clinicians and operations experts whose purpose is to improve clinical outcomes data by reducing data variability associated with lack of training, inconsistent approaches to scale administration and scoring, placebo response, and incorrect source. The members of CAT have extensive industry-related experience stemming from their time working on the site level for sponsors and other service providers. Additionally, the CAT team has conducted more than 75 international Phase I to Phase IV trials and has trained over 7,000 raters.

What you will do

  • Serve as main contact for the eCOA vendor, Sponsor, and Worldwide study team members
  • Manage vendor deliverables and timelines, as they relate to study assessments
  • Negotiate with eCOA vendor and sponsor regarding eCOA scope of work (SOW)
  • Review and identify study trends and proactively work with eCOA vendor and study team to address study specific requirements
  • Conduct risk assessments to study due to vendor deliverable delays, availability of materials, equipment, and translations and related concerns
  • Communicate above risks to study team and Sponsor in a timely manner
  • Identify and liaise with key study functional leads to support eCOA related processes, including but not limited to: CAT team, Project Management (PM), Clinical Operations, Data Management (DM), and Biostatistics
  • Facilitate collaboration between eCOA processes and DM data transfer requirements, eCRF build, and related needs
  • Facilitate collaboration between eCOA vendor mapping specifications and DM and Biostatistics
  • Participate in budget discussions, including Work Order, Change Order, and related inputs
  • Coordinate and obtain sponsor approval for all vendor related costs and document/plan versions
  • Responsible for reviewing and communicating with vendor regarding system change control, closeout, and database lock activities
  • Collaborate with Worldwide study team to manage eCOA study timelines
  • Organize and maintain CAT project files, study mailboxes, documents, sharepoint/portal and designated folders
  • Develop eCOA specific Launch slides with CAT counterparts
  • Organize, arrange, and lead eCOA related meetings with vendor, including Kick Off Meetings, project build meetings, and maintenance meetings
  • Liaise, review, and provide input to all eCOA plans and content
  • Oversee and participate in User Acceptance Testing activities
  • Protocol consultation specific to eCOA
  • Responsible for eCOA requirements gathering


What you will bring to the role

  • Highly organized, detail- and service-oriented
  • Excellent problem-solving skills
  • Excellent project management skills
  • Excellent planning, managing, monitoring, scheduling, and critiquing skills
  • Excellent at meeting timelines consistently and being able to effectively work under pressure
  • Continuously open to constructive, developmental feedback
  • Strong writing and verbal communication skills in order to clearly and concisely present information
  • Strong interpersonal skills in a fast-paced, deadline oriented, and changing environment
  • Strong ability to handle multiple tasks and many administrative details in a fast-paced and constantly changing environment
  • Strong adherence to company policies and procedures
  • Strong self-motivation skills
  • Strong abil

Apply for this role

Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.

Apply Now →Generate Application Kit

Free account required — sign up in 30s

Company

Worldwide Clinical Trials

View company profile →