FSP CRA OPPORTUNITIES WITHIN PHARMACEUTICAL AND BIOTECH COMPANIES Are you looking for a Clinical Research Associate role that can increase the quality and consistency of your work? RBW Consulting is partnered with a global CRO with leading FSP programs
Summary A rare opportunity with moderate days on site travels within the DACH region. Work at one of the fast growing Top global CRO dedicated to a sponsor completely remote. Permanent contract with excellent career development
Summary A rare opportunity with moderate days on site travels within the DACH region. Work at one of the fast growing Top global CRO dedicated to a sponsor completely remote. Permanent contract with excellent career development
Position: CRA II Location: Remote across Germany Company: Mid-sized CRO (2000+ employees) Salary: €60,000 - €65,000 Therapy Areas: Oncology, Haematology, & Infectious Diseases Site visits: 6 per month on average RBW Consulting are excited to announce
Summary A completely remote opportunity with moderate days on site travels within the DACH region. Work at one of the fast growing Top global CRO dedicated to a sponsor. Permanent contract with excellent career development options.
RQM+ is the largest global MedTech CRO, offering consulting, clinical trial, lab and reimbursement services across the entire product lifecycle. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and
RQM+ is the largest global MedTech CRO, offering consulting, clinical trial, lab and reimbursement services across the entire product lifecycle. We accelerate the success of medical device, IVD, and combination product companies by providing industry-leading regulatory and
Job summary: Have you ever thought about having a new job for the year 2023? By simply clicking apply or contacting me, you wil enjoy the following benefits: Customized consultative assistance in Job search Assistance throughout
Was würden Sie gerne an Ihrem Job ändern? Klicken Sie einfach auf Bewerben oder nehmen Sie Kontakt mit mir auf und genießen Sie die folgenden Vorteile: Maßgeschneiderte beratende Unterstützung bei der Jobsuche Unterstützung während des gesamten
Position: Senior Clinical Research Associate Germany Erfahrung: 1-3 Jahre als Senior Clinical Research Associate Ort: Deutschland (remote) Sind Sie sich sicher, dass Sie auch wirklich den Job haben, der Sie zu 200% zufrieden macht? Sie haben auch nur die kleinste Überlegung daran,
Position: Senior Clinical Research Associate Germany - Sponsor Dedicated Erfahrung: 1-3 Jahre als Senior Clinical Research Associate Ort: Deutschland (remote) Sind Sie sich sicher, dass Sie auch wirklich den Job haben, der Sie zu 200% zufrieden macht? Sie haben auch nur die
Job summary: Are you 120% sure you are having your dream job ? By simply clicking apply or contacting me, you wil enjoy the following benefits: Customized consultative assistance in Job search Assistance throughout the whole
The Clinical Research Associate will perform site activities for Phase I-IV studies operating as the main point of contact for the site during a study. Drive and execute monitoring plans, ensure site GCP compliance, write trip reports, resolve issues
Current Employees: If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply
Current Employees: If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health
Current Employees: If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply
REMOTE WORKING OPPORTUNITIES AVAILABLE ACROSS GERMANY AND UNITED KINGDOM Main Responsibilities Acting as Global Regulatory CMC Lead to define and execute the CMC regulatory strategy from clinical development up to market authorisation. Plan, prepare, and conduct interactions
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health
Clinical Operation Manager - Medical Device industry Are you a Line Manager who is keen to join a fast growing industry in a established and dynamic company? Then I have the right opportunity for you! I am