Associate Director, Pharmacology at ALKAbell
Hørsholm, Region Hovedstaden, Denmark -
Full Time


Start Date

Immediate

Expiry Date

03 Aug, 25

Salary

0.0

Posted On

03 May, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

A
s Associate Director, Pharmacology, you will join ALK Global Research as responsible for the pharmacological research aligned with ALKs overall strategy and lead a team of highly experienced scientists and technicians. You will take seat in the Drug Discovery Management Team and report to the VP of drug discovery.
You will participate in and oversee the design and execution of preclinical and clinical PK/PD pharmacology studies to assess drug efficacy, mode of action, safety, and pharmacokinetics and ensure adherence to regulatory guidelines and industry best practices. Furthermore, you will participate in managing third party CROs that provides non-clinical services, communicate with regulatory authorities, and convey, adapt and influence internal stakeholders on pharmacological issues.

Your primary tasks will be to:

  • Provide guidance, mentorship, and professional development opportunities for team members.
  • Develop and implement a pharmacology strategy aligned with ALKs overall research and development goals.
  • Guide the selection of animal models and study designs including related in vitro/ex vivo analyses.
  • Analyse and interpret pharmacology PK/PD data, drawing meaningful conclusions and making recommendations for further drug development.
  • Collaborate with internal and external stakeholders, including scientists, regulatory affairs, and clinical development teams.
  • Collaborate with cross-functional teams to ensure alignment with project objectives.
  • Effectively communicate pharmacological findings to diverse audiences, including senior management and regulatory agencies.
  • Stay updated with evolving regulatory requirements and ensure that pharmacology studies meet regulatory standards.
  • Manage departmental budgets.

BECOME A PART OF ALK

We provide an attractive working environment for individuals looking for both personal and professional development. ALK is a global pharmaceutical company specialised in allergy immunotherapy. We are driven by a high level of professionalism, integrity, an open-minded approach and contributing to an inspiring and fun working environment together with our colleagues.
ALK provides a uniquely dynamic and pleasant work environment, complete with inspiring and challenging assignments. You will be part of an engaged and informal team who values skill and knowledge creation. The result of your efforts will be significant throughout the organisation, and you will be able to actively influence and challenge the status quo.
Our offices in Denmark offer a green view of the DTU Science Park in Hørsholm. We believe that physical presence enforces strong teamwork and collaboration and creates success, so it is important that you enjoy coming to work at our site with a degree of flexibility to also work from home from time to time.
Do you want to learn more about our company, we encourage you to visit us at www.alk.net.

Responsibilities
  • Provide guidance, mentorship, and professional development opportunities for team members.
  • Develop and implement a pharmacology strategy aligned with ALKs overall research and development goals.
  • Guide the selection of animal models and study designs including related in vitro/ex vivo analyses.
  • Analyse and interpret pharmacology PK/PD data, drawing meaningful conclusions and making recommendations for further drug development.
  • Collaborate with internal and external stakeholders, including scientists, regulatory affairs, and clinical development teams.
  • Collaborate with cross-functional teams to ensure alignment with project objectives.
  • Effectively communicate pharmacological findings to diverse audiences, including senior management and regulatory agencies.
  • Stay updated with evolving regulatory requirements and ensure that pharmacology studies meet regulatory standards.
  • Manage departmental budgets
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