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Associate Director, GCP/PV

Genmab



Associate Director, GCP/PV

Genmab is an international biotechnology company specializing in the invention and development of differentiated human antibody therapeutics for the treatment of cancer and other important human diseases.

The Role

You will work in a multidisciplinary international QA team to ensure compliance to industry standards and regulations. As Associate Director, GCP/PV you will conduct audits internally as well as externally at our CRO’s and collaborators. You are responsible for writing audit reports and review audit responses to audit closure. In addition, you will provide support to the clinical teams regarding GCP and regulatory requirements within the area of clinical trials conduct and be the acting chair in SOP committees.

As part of the QA department, you are an active collaborator within Genmab.

Responsibilities

The responsibilities of the Associate Director, GCP/PV will include, but not be limited to:

  • Be an active QA representative in both the early and late stage clinical development and for the marketed products, including oversight of GCP and Drug Safety activities globally
  • Plan, perform and follow-up on Quality Audits within GCP and Drug Safety/PV regulated areas both internally and externally and perform vendor evaluations
  • Represent QA in clinical project groups or clinical sub groups and participate in cooperation with partners and contractors as appropriate
  • In addition to this, the employee shall provide internal QA support in the organization and prepare/coordinate
  • Participate in GCP/PV inspections performed by national authorities
  • Clinical and drug safety/PV Quality Agreements
  • Participate in the development and maintenance of the existing Quality Management System (QMS) and associated GCP and PV SOPs
  • Participate in knowledge sharing by gaining and maintaining expert knowledge about new GCP and drug safety guidelines, clinical trials laws, legislations and practices, including informing relevant parts of the organization
  • Participate in training and education of employees in the GCP, drug safety and other relevant guidelines and regulations, and ensure oversight of the company’s clinical trials is conducted in compliance with clinical protocols, GCPs and other regulatory requirements
  • Experience with oncology will be beneficial

Requirements

  • You hold an MSc in Pharmacy or a related scientific degree, or alternatively otherwise medically trained
  • You have more than five years relevant industry experience in the GCP and Drug Safety areas working in a Quality department
  • You have experience in SOP training
  • You have experience working in an EDMS system, such as Veeva Vault document management
  • You have excellent communication skills in both English and Danish, and a collaborative mind-set
  • Experience of oncology, late phase, pharmacovigilance, and/or first in human trials would be beneficial
  • You are willing to travel globally for up to 20% of your work schedule
  • Trained auditor is beneficial

In case you have any question, please feel free to reach out to Recruiter Jannie Jensen at jjn@genmab.com

Genmab employees work with determination and with respect for each other, consistent with our core values, to achieve our common goals. We give individuals and teams the autonomy to drive development of innovative products and solutions, knowing that integrity is a core value throughout our company. Genmab will offer the successful application a challenging position, where the right candidate will have the opportunity to work with highly specialised people across functions in an informal, multicultural culture, all aiming to make a difference for cancer patients.

Teamwork and respect are central pillars of Genmab’s culture and we therefore ensure an inclusive, open, and supportive professional work environment across our international locations. We believe that fostering workplace diversity across social, educational, cultural, national, age and gender lines is a prerequisite for the continued success of the company. We are committed to diversity at all levels of the company and strive to recruit employees with the right skills and competences, regardless of gender, age, ethnicity, etc.

Please note that if you are applying for a position in the Netherlands; Genmab’s policy for all permanently budgeted hires in this location is to offer a temporary agreement for one year, followed by a contract for indefinite time regardless of seniority.

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Genmab
Genmab
Genmab is a publicly traded, international biotechnology company specializing in the creation and development of differentiated antibody therapeutics for the treatment of cancer. Founded in 1999, the company has three approved products in collaboration, a broad clinical and pre-clinical product pipeline and four proprietary next generation antibody technologies.

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Kalvebod Brygge 43
1560 København V
Logo: Genmab
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