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 The Operations Manager Does At Worldwide The Operations Manager has primary responsibility for overseeing the operational work related to rater selection, rater certification/qualification, rater training content, scale acquisition, surveillance maintenance, and workbook/source document management for Worldwide Clinical Trials, Inc. (Worldwide). The Operations Manager is responsible for ensuring all assigned projects are conducted in a timely fashion and in a manner compliant with Standard Operating Procedures (SOPs),



International Council for Harmonization/Good Clinical Practice (ICH/GCP), and regulatory guidelines. The Operations Manager works under the direction of the Operations Director, Clinical Assessment Technologies (CAT).

What You Will Do

Coordinate completeness of rater experience qualification documents and communicate collection results to the Sponsor and study team

Develop study‑specific rater training web portals and ensure readiness based on study timelines

Coordinate logistical matters of the Investigators’ Meetings and associated CAT materials; manager may attend such meetings

Organize the timely completion of editing and formatting of didactic training presentations

Oversee scale and study source workbook management by obtaining scale licenses, translations, regulatory authorizations, and Sponsor approvals

Oversee data surveillance methodology maintenance by tracking and reconciling incoming source documentation and providing reports to the study team and Sponsor

Provide necessary CAT data to ensure comprehensiveness of CAT’s Final Study Report

Oversee archiving of all CAT study documents

Consult on rater training and data surveillance plans to ensure documents represent Sponsor and protocol specifications

Other Clinical Assessment responsibilities

May develop and present at Sponsor Kick-Off Meetings regarding CAT operations work





Work with the Operations Director and Worldwide Clinical Trials study team to ensure study budgetary demands are met

Manage Operations staff, as assigned

Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all‑inclusive.

What You Bring To The Role

Highly organized, detail‑oriented, and service‑oriented

Excellent planning, managing, monitoring, scheduling, and critiquing skills

Excellent at meeting timelines consistently and effectively working under pressure

Continuously open to constructive, developmental feedback

Strong writing and verbal communication skills 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 administrative details in a rapid‑paced and constantly changing environment

Strong self‑motivation skills

Strong ability to work in teams

Excellent proficiency in all Microsoft Office applications, including Microsoft Word, Excel, Adobe, and PowerPoint

Your Experience

Bachelor’s degree in Life Science preferred

Two to four years of experience working in clinical trials

At least two years of experience managing team members or leading a team. In lieu of people management experience, the individual must demonstrate a strong ability to lead, understand policies and procedures, financial and leadership principles, possess excellent time management and project management skills, and communicate effectively

Demonstrable knowledge of operational as

📌 Manager, Clinical Assessment Technologies Operations (Iqaluit)
🏢 Worldwide Clinical Trials
📍 Iqaluit