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Clinical Team Manager

Ergomed

Toronto

Remote

CAD 80,000 - 100,000

Full time

Today
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Job summary

A global clinical research organization in Toronto is seeking an experienced Clinical Team Manager. You will manage site-level operational study tasks, ensuring compliance and training of team members. The ideal candidate will have extensive experience in multiple clinical studies, particularly in complex trials like oncology. This role fosters a supportive work environment with a focus on diversity and inclusion, offering career development opportunities and flexible work options.

Benefits

Training and career development opportunities
Friendly supportive working environment
Opportunity to work globally with English as the company language

Qualifications

  • Extensive clinical research lead experience in multiple studies.
  • Experience in managing the clinical part of studies in multiple regions.
  • Experience of phase 2 / 3 trials, ideally oncology or rare disease.

Responsibilities

  • Responsible for site level operational study management.
  • Identify, resolve, and escalate risks or issues to project management.
  • Ensure project team members are trained on procedures and protocols.

Skills

Clinical research lead experience
Project management
Spanish language skills

Education

Science-based bachelor's degree
Job description
Responsibilities

The Clinical Team Manager will be responsible for site level operational study management

The CTM proactively identifies, resolves / mitigates and escalates risks and / or issues to the PM / PD and Head of Clinical Operations as necessary

Verifying and ensuring that project team members (CRAs Site Managers CTAs) are trained (e.g. GCP SOP indication protocol study specific procedures / requirements etc.) to perform their assignments

Developing, reviewing and revising project documents (e.g. clinical monitoring plan, CRF completion guidelines, study specific operating manual, study specific forms etc.)

Initiating corrective / preventative measures e.g. updating study guidance documents, performing re‑training, performing co‑monitoring etc.

Qualifications
  • Extensive clinical research lead experience in multiple studies
  • Experience in managing the clinical part of studies in more than one region or equivalent study complexities
  • Experience of phase 2 / 3 trials, ideally complex studies such as oncology or rare disease
  • Able to work in a fast‑paced small CRO environment and manage multiple projects
  • Spanish language skills and experience in LATAM preferred
  • A minimum of a science‑based bachelor’s degree
  • Able to work effectively with minimal supervision
Additional Information
Why Ergomed

We prioritize diversity, equity and inclusion by creating an equal opportunities workplace and a human‑centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.

To succeed we must work together with a human‑first approach. Why because our people are our greatest strength leading to our continued success on improving the lives of those around us.

We offer
  • Training and career development opportunities internally
  • Strong emphasis on personal and professional growth
  • Friendly supportive working environment
  • Opportunity to work with colleagues based all over the world with English as the company language
Values
  • Quality
  • Integrity & Trust
  • Drive & Passion
  • Agility & Responsiveness
  • Belonging
  • Collaborative Partnerships

We look forward to welcoming your application.

Remote Work

Yes

Employment Type

Full‑time

Key Skills
  • Computer Hardware
  • Fund Management
  • Attorney At Law
  • Jni
  • Analytics
Experience

years

Vacancy

1

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