Clinical Team Manager

Ergomed

$90K — $120K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Extensive clinical research lead experience in multiple studies
  • Experience managing clinical studies across multiple regions
  • Experience with complex phase 2/3 trials, ideally in oncology or rare diseases
  • Ability to thrive in a fast-paced small CRO setting
  • Minimum of a science-based bachelor's degree
  • Ability to work independently with minimal supervision

Responsibilities

  • Oversee operational project management for clinical studies
  • Proactively identify and address risks and issues in projects
  • Ensure project team members are trained on relevant protocols and procedures
  • Develop and revise project documentation such as clinical monitoring plans
  • Initiate corrective measures including updates to study guidance and retraining

Benefits

  • Training and career development opportunities
  • Strong focus on personal and professional growth
  • Supportive and friendly working environment
  • Global collaboration with colleagues, primarily in English
Full Job Description
Job Description

Responsibilities:
  • The Clinical Team Manager will be responsible for operational project 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 revision of project documents (e.g., clinical monitoring plan, CRF completion guidelines, study specific operating manual, study specific forms etc.)
  • Initiating corrective / preventative measures - e.g., update of study guidance documents, performing re-training, performing co-monitoring, etc.


Qualifications

  • Extensive clinical research lead experience in multiple studies
  • Experience in managing 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
  • 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

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