Clinical Team Manager

Ergomed

$90K — $120K *
US-AnywhereRemote in Raleigh, NC
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Extensive experience leading multiple clinical research studies.
  • Managed clinical aspects of studies across various regions or complexities.
  • Proven track record with phase 2/3 clinical trials, particularly in oncology or rare diseases.
  • Ability to thrive in a dynamic, small CRO environment managing multiple projects.
  • Bachelor's degree in a science-related field is required.
  • Capacity to operate effectively with minimal supervision.

Responsibilities

  • Oversee operational project management of clinical trials.
  • Proactively identify, resolve, and escalate risks to relevant stakeholders.
  • Ensure project team members are properly trained in necessary protocols and guidelines.
  • Develop and revise critical project documentation for clinical studies.
  • Initiate corrective measures to address guidance documents and conduct necessary training.

Benefits

  • Opportunities for training and career advancement within the company.
  • Strong emphasis on personal and professional development.
  • Supportive and friendly work environment.
  • Networking opportunities with colleagues globally, using English as the business language.
Full 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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