Senior Project Manager

Ergomed

$90K — $130K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 5-7 years of experience as a Project Manager in an international clinical trials setting within a CRO
  • In-depth knowledge of Oncology and Rare Disease therapeutic areas
  • Proficient in selecting and managing external service providers
  • Strong analytical, organizational, and communication skills
  • Bachelor's Degree in a science-related discipline.

Responsibilities

  • Ensure timely, budget-compliant delivery of projects according to quality standards
  • Liaise with project team members and provide necessary training for task allocation
  • Develop and edit project plans to align with project goals and milestones
  • Organize and facilitate project meetings for study activities
  • Serve as the primary contact for project status with sponsors and senior management
  • Represent the company at external meetings, engaging with scientific experts and committees
  • Develop and edit SOPs to ensure regulatory compliance and create training programs.

Benefits

  • Opportunity to make a meaningful impact in global healthcare
  • Join a passionate and collaborative team of clinical research experts
  • Work in a value-driven environment focused on integrity, quality, and patient outcomes
  • Access a diverse workplace that values every voice
  • Engage in collaborative partnerships that enhance project efficacy.
Full Job Description
Job Description
  • Ensure that projects are delivered on time, within budget, and agreed scope, maintaining the appropriate industry, sponsor and Ergomed quality standards
  • Liaise with project team members, provide training where needed and ensure correct allocation to tasks
  • Develop, review and edit project plans to assure consistency with goals and milestones
  • Organization and facilitation of project meetings related to study activities (study organization, initiation, execution, closure)
  • Serve as primary point of contact with sponsor and Ergomed Senior Management on project status
  • Represent Ergomed at external meetings, providing liaison with scientific/medical experts in other CRO/Sponsor companies and for committee meetings, (e.g.EC/IRB)
  • Develop review and edit of relevant SOPs to assure consistency with Regulatory standards and develop study related training programs to support this.
  • Contribute to bid defense activities


Qualifications

  • Experience serving as a Project Manager of international clinical trials in a CRO environment
  • Knowledge of Oncology and Rare Disease therapeutic areas
  • Experience in selecting and managing external service providers
  • Strong analytical, organizational and communication skills
  • Bachelor's Degree in a science related discipline.


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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