id: NDk1NTg1NiA3

reference: 4955856

documentId: 4955856

connectionPointId: 7

lastModificationDate: 1551949946160

stillingsbetegnelse: Clinical Site Agreement Manager

jobbeskrivelse:

Can you manage business critical clinical trial agreements on a global scale?

If you bring clinical contract experience and you are motivated by playing an important role in taking a global company to the next level within your area of expertise, this job is your perfect match. LEO Pharma has set the very ambitious goal to become the world’s preferred dermatology care partner. A top class clinical trial set up is a cornerstone in making this come true, and that is why we need you and all of your skills across strategy, contracts and negotiations.

Strategy, contracts, negotiations, process optimization…
As Clinical Site Agreement Manager you are responsible for drafting, developing and negotiating site contracts for clinical trials worldwide. You are in charge of the strategy, negotiations, resolutions and escalations of contract and budget issues to the relevant internal stakeholders. Your primary tasks will be to:

• Negotiate and execute clinical site agreements
• Review wording of site contracts and budgets and provide input 
• Manage issues and risks for individual trials by addressing contract challenges and evaluating site budget escalations
• Develop a new site agreement strategy, oversee and optimize the process
• Build and maintain reporting tools aimed for Clinical Project Managers and Leadership Team
• Evaluate country level budget strategy 
• Monitor trends and refine existing guidance, tools, and templates

You will support and be in contact with multiple colleagues and partners including Clinical Project Managers, Clinical Research Associates, Trial Execution, medical and legal departments and the Global Clinical Operations Leadership Team. For this, you will need your ability to shape your communication to fit your audience across cultural and professional borders.

Contract experience and clinical understanding from pharma/biotech/healthcare
You hold a university degree in Law, Economy, Business Administration or science, and you are used to drafting and negotiating site contracts and/or site budgets. As part of this, you can handle negotiations, make decisions and present your recommendations and results in an easy understandable way, in written and spoken English. Your career has also provided you with at least 3 years’ pharma/biotech/healthcare experience from working with clinical development, GCP, relevant ICH standards, and FDA/EMA guidelines.

To succeed, you will need a sense of details and ability to ensure correct information in your documents. You must thrive on being trusted with major responsibility and be able to move things forward no matter if you are working on your own or as part of a team. Additionally, you must be able to hold your ground while collaborating with highly competent stakeholders in high-level positions.

Your new team

You will join our Site Agreement Management team at the LEO Pharma Headquarters in Ballerup, Greater Copenhagen. We are currently two in Ballerup and three at our New Jersey office in Madison. The team is responsible for managing all contracts relating to the conduct of clinical trials on a global scale.

We look forward to receiving your application.

numberOfPosts: 1

jobCategoriesCodes_0: http://data.europa.eu/esco/isco/C1211

abstractJV_contact_0: Please apply using one of the specified channels

positionTypeCode: directhire

contractTypeCodes_0: fulltime

Arbejdsgiver Navn: LEO PHARMA A/S

source: DK-STAR