CDC Trial Manager

2 tygodni temu

Warszawa, Mazovia, Polska Novo Nordisk Pełny etat

Job Description:

In the role of CDC Trial Manager, you will focus on developing and executing all stages of the allocated Trial Strategic Plan at the CDC level. On a daily basis, your responsibilities will include managing allocated trials on the CDC level to deliver the trials' KPIs, overseeing CDC Trial Teams, establishing and maintaining professional relationships with internal and external stakeholders, and carrying out additional responsibilities defined by your line manager.

Your key responsibilities will involve:

  1. Supporting the development and implementation of CDC level Trial Strategic Plans and, if necessary, Risk Management Plans for all trials under your responsibility.
  2. Driving patient relocation in close collaboration with adjacent affiliates.
  3. Organizing kick-off meetings with CDC Trial Team members (Start-up CRAs, CRAs, and CTAs), following up on their progress, and escalating identified issues/challenges to appropriate stakeholders as needed.
  4. Performing TM monitoring, creating and reviewing trial country and CDC budgets, and approving trial-related payments.
  5. Supporting CRAs by performing co-visits, organizing pre-audit meetings, reviewing and approving all types of site visit reports, approving GL forms, and performing IMPACT quality checks.
  6. Building and maintaining relationships within the CDC Trial Team and the Trial Squad, and acting as a leader for all CDC Trial Team members regarding trials under your responsibility.
Qualifications:

To be successful in this role, you need to possess excellent communication and presentation skills, the ability to build relationships with various stakeholders, negotiation skills, and influencing skills. The following qualifications are also required:

  • Master's degree in Life Science or similar field.
  • Fluency in English – written and spoken.
  • Minimum 3 years in the clinical research industry.
  • Previous CRA experience is preferred.
  • Minimum 6 months of experience in project management of clinical trials.

Other essential attributes include proactivity, the ability to work in a changing environment, impact and influence others to achieve shared goals without using formal power or coercion, team orientation, flexibility, cross-cultural awareness, and problem-solving skills.

About the Department:

CDC Poland is part of Region South East Europe, Middle East, and Africa (SEEMEA) and is a new clinical organization within Novo Nordisk Poland. Responsible for conducting clinical trials across multiple countries, CDC Poland provides clinical trial management and administration support to adjacent Affiliates and currently oversees approximately 20% of global patients in Novo Nordisk clinical trials.

Working at Novo Nordisk:

Novo Nordisk values its employees for the unique skills they bring to the table and is committed to bringing out the best in them. Working at Novo Nordisk means working toward something bigger than oneself through the collective effort of more than 63,000 employees, making life-changing impacts.


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