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Time for a change - time for a new job! Are you a Clinical Biosample Operations Expert looking for a new professional challenge? Then stop looking! We offer you the job you are looking for: a secure job, fair remuneration and exciting new tasks in an attractive pharmaceutical company in Biberach. Apply online now - quickly and easily! We value equal opportunities and welcome applications from people with disabilities.
Direct recruitment is possible.
Das dürfen Sie erwarten
- Attractive salary based on the BAP/DGB collective agreement
- Reliable and punctual payment, possibility of monthly partial payments
- Attractive social benefits, such as vacation and Christmas bonuses
- Option of permanent employment with our business partner
- Extensive social benefits, incl. Christmas and holiday bonuses
- Up to 30 days vacation per year
- Representation of interests by a comprehensive works council
- Challenging projects and diverse tasks in an international environment
- A wide range of employee benefits/perks
- Thorough induction/training provided by our client company
- Use of the Randstad App (leave requests online, payroll viewable at any time and much more)
Ihre Aufgaben
- In your new role, you are responsible to design, setup, coordinate and monitor the logistical part of clinical trials for biosamples (pharmacokinetic, biomarker and biobanking) on a global level.
- You ensure that clinical sites are properly equipped, supported and trained for sampling, sample handling and processing, storage and shipments of the biosamples.
- You work together with international external partners and vendors.
- Being a member of the international clinical trial teams, you work according to GCP, contribute to relevant study documentation, support the data reconciliation between central lab and study databases and participate in international meetings.
- You work together with trial leads, monitors, data managers, pharmacokineticists, bioanalysts and biomarker experts and other relevant functions involved in the clinical studies.
- Additional to the trial work, you drive the revision and development of relevant internal processes and infrastructure.
- You are responsible for highly complex clinical trials and supervise Junior CBO Experts
- You chair international meetings and train relevant interface parties
- You drive and implement Innovation & process improvements
Unsere Anforderungen
- Completed Master degree in a medical-scientific subject or equivalent education with several years of working experience
- Basic knowledge and experience in the area of laboratory analytics for samples/material from clinical studies, as a clinical research associate or other experience in the area of clinical studies
- GCP knowledge and good knowledge of MS Office applications
- Independent, collaborative and structured work style with outstanding interpersonal and communication skills
- Innovative mindset to work effectively in a fast changing environment. Strong team player with excellent communication skills – capable of working in multi-disciplinary and global teams.
- Excellent English - both spoken and written
- Specialist knowledge and several years of experience in the area of laboratory analytics for samples/material from clinical studies, as a clinical research associate or other experience in the area of clinical studies
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