Clinical Team Manager

Ergomed

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

Qualifications

  • Extensive clinical research lead experience across multiple studies
  • Experience managing clinical trials in various regions or complex study settings
  • Experience with phase 2/3 trials, especially in oncology or rare diseases
  • Ability to handle multiple projects in a fast-paced small CRO environment
  • Minimum of a science-based bachelor's degree
  • Capability to work effectively with minimal supervision

Responsibilities

  • Manage operational project management for clinical trials
  • Identify and resolve project risks and issues proactively
  • Ensure project team members are properly trained on relevant protocols and regulations
  • Develop and revise project documentation, including monitoring plans and guidelines
  • Implement corrective and preventative measures as necessary

Benefits

  • Opportunity to significantly impact patient care
  • Join a passionate and collaborative expert team
  • Work in a values-driven environment that promotes quality and integrity
  • Opportunity for growth in a dynamic small CRO setting
  • Diversity and inclusion in the workplace
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

When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. You'll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.

We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here.
  • Quality: we hold ourselves to the standard patients deserve.
  • Integrity and trust: we do the right thing, especially when it is hard.
  • Drive and passion: we care about the outcome, because someone is waiting on it.
  • Agility and responsiveness: we move quickly, because patients cannot wait.
  • Belonging: everyone is welcome, and every voice counts.
  • Collaborative partnerships: we go further by going together.

We look forward to welcoming your application.

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