Project Manager Clinical Studies m/f/x

Argenta; Deutschland; Vor Ort; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

An established industry player in animal health is seeking a Project Manager to join their dynamic team. In this role, you will oversee the planning and execution of clinical studies, ensuring that projects are conducted efficiently and effectively. Your responsibilities will include training study participants, conducting site visits, and managing budgets. The ideal candidate will have a background in veterinary medicine or pharmacy, strong communication skills in both German and English, and a passion for working in a collaborative environment. If you are eager to take on new challenges and contribute to impactful projects, this is the perfect opportunity for you.

Qualifikationen

• Graduate in veterinary medicine or pharmacy with clinical research experience.
• Strong communication skills in German and English are essential.

Aufgaben

• Plan and execute clinical studies at national/international level.
• Manage project budgets and organize study drugs.

Kenntnisse

Veterinary medicine

Pharmacy

Clinical research

Communication skills

Project management

Ausbildung

Degree in veterinary medicine

Degree in pharmacy or comparable science

Jobbeschreibung

Companies in the animal health and feed industries require qualified support in the development and registration of their products.

ARGENTA is the number one contract development and research organization dedicated exclusively to the animal health industry, with sites in New Zealand, the USA and Europe. In Europe, our clinical research and development services are provided from our offices in Munich, San Sebastian and Barcelona. In recognition of our long history of providing these services, Argenta and its German subsidiary, KLIFOVET GmbH, have been awarded several times since 2006 as the best service provider in the animal health sector internationally.

About the role

This Project Manager role will be an active team member.

You will be responsible for:

1. Planning and execution of clinical studies at national/international level
2. Selecting, training, and supervision of the study participants involved
3. Conducting site visits
4. Preparing study protocols and reports for our clients
5. Planning data analysis and quality controls
6. Organizing and managing study drugs
7. Managing the project budget

About you

A graduate in veterinary medicine, pharmacy or comparable science, ideally followed with experience in veterinary practice and/or clinical research.

You will be:

1. Keen to learn new tasks and build upon areas of knowledge
2. Capable of working independently with a structured approach to tasks
3. Agile and flexible with a high sense of responsibility
4. Possessing strong written and verbal communication skills including a good command of German and English
5. A willing and credible team player with a distinctive customer orientation
6. Willing to travel for business (approx. 30% of working time)

If you are looking for your next role and can meet the above criteria, we'd love to hear from you!