Project Manager Oncology experience required

Ergomed; Raleigh (NC); On-site; USD 90,000 - 130,000; Full time

Job summary

Ergomed is seeking a Project Manager to lead international clinical trials from our Raleigh office. You will ensure on-time, on-budget delivery within scope, liaising with sponsors, study teams and Ergomed senior management.

This role requires a science degree and experience in CRO environments with Oncology or Rare Disease programs. You will develop project plans, organize study meetings and help manage external vendors, contributing to bid defenses.

Qualifications

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

Responsibilities

• Ensure delivery of projects on time, within budget and scope.
• Liaise with project team, provide training where needed and ensure correct allocation to tasks.
• Develop, review and edit project plans to align with goals and milestones.
• Organize and facilitate study-related meetings (organization, initiation, execution, closure).
• Serve as primary contact with sponsor and Ergomed Senior Management on status.
• Represent Ergomed at external meetings with scientific/medical experts and committees.
• Develop and review SOPs to ensure regulatory compliance and training.
• Contribute to bid defense activities.

Skills

Analytical skills

Organizational skills

Communication skills

Education

Bachelor's Degree in a science related discipline

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.