HBS Compliance Specialist at AstraZenca Gothenburg

Do you want to work with fundamental research? AstraZeneca in Gothenburg are looking for a HBS Compliance Specialist!

Are you analytical and have good communication skills? Do you want to Co-ordinate projects and assist in delivery to ensure collation of all information related to HBS? Apply today for the role as a HBS Compliance Specialist at AstraZeneca in Gothenburg!

Human Biological Samples (HBS) are fundamental to medical research in the discovery, development and implementation of new treatments and diagnostics. HBS are ethically sensitive materials and the collection, handling, and access to HBS are subject to strict regulations, principles and ethical guidelines.

Purpose, Offer and Benefits

This is an exiting oppurtunity to work with medical research in a company wich strategy are to focus  on creating genuinely innovative medicines and improving access to them.

Your Responsibilities

Day-to-Day Duties

• Co-ordinate projects and assist in delivery under the supervision of the Biobank lead and/or Compliance manager to ensure collation of all information related to HBS.
• The post holder may be required to work in the biobank to reconcile the HBS inventory or knowledge curation to allow decision making on inventory.
• Collaborate with the internal teams in locating samples and reviewing consent for requests related to HBS in AZ.
• Assist in knowledge curation to allow decision making on inventory which maybe in AZ, or third parties. Duties may include handling of HBS during the reconciliation and curation process.
• Work with the Biobank lead to ensure that learning from HBS related issues are identified and analysed to enable continuous process improvement.

The Bigger Picture

This position is a consultant assignment. The assignment is a full-time job and will last for 6-12 months! The start date for this position will be ASAP:.

You will be employed by TNG Group during this assisgnment.

Our Expectations

 Experience/ Education/ Qualifications:

• Bachelor´s degree level education
• 6 months of relevant experience
• Excellent analytical, written, and oral communications skills.
• Proven team working skills
• Ability to work independently
• Project management experience and skills
• High ethical standards, trustworthy, operating with absolute discretion

We would also like to see that you have, knowledge and understanding of compliance function, health care regulations, laws, and standards and have some experience in pharmaceuticals or a related industry. It is desirable if you have experience with administrative tools such as excel and SAP.