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Clinical Site Manager (fluent German speaker required)

ErgomedFrankfurt | Hesse, GermanyRemote
This job is no longer open

Company Description


This position requires a German speaker but you can be based anywhere in the EU/UKErgomed CR is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease.  Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia Our company allows for employee visibility (you have a voice!) creative contribution and realistic career development.  We have nourished a true international culture here at Ergomed.  We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved. Come and join us in this exciting journey to make a positive impact in patient’s lives.  

Job Description


  • Training, consultation and support of Study Site Coordinators /Research Nurses on clinical studies
  • Providing non-operational site support to ensure progress of clinical study and to ensure that it is conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH GCP, and the applicable regulatory requirement(s)
  • Notifying Study Monitor / Team on any site issues that are detected in contact with the clinical center and are relevant for them
  • Establishing and maintaining relationships with Study Site Coordinators and Investigators to optimize performance of clinical study
  • Assistance in development of recruitment strategies and tracking of recruitment or patient retention activities at the site

Qualifications


  • Bachelor or Master of Science degree or equivalent (preferably in medical field, i.e. medical nurse)
  • Experience as a Clinical site manager, Study nurse or study site coordinator
  • Excellent organisation skills with attention to detail
  • Excellent interpersonal and communication skills
  • Good IT skills (MS Word, Excel, Internet tools)

Additional Information


We offer excellent chances to progress and develop. We work on a global basis on interesting projects within rare diseases, oncology, and neurology. This is an ideal position to continue developing a career in clinical drug development.We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.  To succeed we must work together with a human first approach.

Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us.  We offer: 


  • Training and career development opportunities internally  

  • Strong emphasis on personal and professional growth 

  • Friendly, supportive working environment 

  • Opportunity to work with colleagues based all over the world, with English as the company language 

Our core values are key to how we operate, and if you feel they resonate with you then Ergomed is a great company to join!  Quality Integrity & Trust  Drive & Passion  Agility & Responsiveness  Belonging Collaborative Partnerships  We look forward to welcoming your application. #LI Remote

This job is no longer open

Life at Ergomed

Founded in 1997, Ergomed is a global provider of high-quality services to the biopharmaceutical industry, spanning all phases of clinical trials, post-approval pharmacovigilance, and medical information. Ergomed’s fast-growing services business includes an industry-leading suite of specialist pharmacovigilance (PV) solutions, integrated under the PrimeVigilance brand, and Ergomed Clinical Research, a complete, global Phase I-IV clinical development and trial management services with a strong heritage in the development of drugs in rare diseases and oncology. • 1,400+ highly qualified professionals • Global full-service CRO • 25+ years of experience • Therapeutic specialization in oncology • Strong expertise in rare disease trials • Robust clinical safety system • Choice of leading drug safety databases Our key services include: • Clinical Research Services • Pharmacovigilance • Medical Information • Regulatory • Medical Writing • Site Management • Study Physician Support • Biostatistics • Patient Study Support
Thrive Here & What We Value1. Emphasis on personal and professional growth2. Friendly, supportive working environment3. Opportunity to work with colleagues globally (English as company language)4. Diversity, equity, inclusion, equal opportunities5. Human-first approach for success6. Employee visibility and creative contribution7. Realistic career development8. Healthy work-life balance
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