Výsledky vyhledávání: 11 pracovních nabídek
...and responsible for study cost-effectiveness
• Dependent on level of experience you may assist in training and mentoring less expert CRA’s and/or lead CRA’s working on international projects
What you need :
• 12 months+ of monitoring experience in pre and post...
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...to assist in training and mentoring fellow CRAs
You will need:
• 18 months+ of monitoring experience in phase I-III trials as a CRA
• College degree in medicine, science, or equivalent
• Previous monitoring experience in medium-sized studies, including study start...
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...monitoring? Are you looking for your next step in your career? If yes, we have an excellent opportunity for you! We are now hiring one CRA (or Senior CRA) and we will have more openings soon. That's why we made this opportunity for you.
By joining our pipeline, you...
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Odpoledne směna
...oversight, and compliance check of e-TMF for assigned clinical trials in close collaboration with CDC CTA and track site trainings through CRA responsible.
Control the accuracy of the trial data based on DM reports in the systems and follow up with CRAs towards DBL. Review...
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Flexibilní pracovní doba
...Clinical System Implementation Manager to join our dynamic team in Prague! Could it be you?
The ideal candidate will come from a Senior CRA or Trial Manager background and have experience in managing the implementation of clinical systems and software solutions. As a...
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...develop and grow your career even further, then this is the opportunity for you.
Responsibilities
We are looking for a CRA with experience responsible for the following:
Conduct qualification, initiation, monitoring, and closeout visits for research...
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...Associates possess varied backgrounds in medical and other science-related healthcare fields. Individuals who have succeeded in the CRA role include:
Nurses
Pharmacists
PhD/Pharm.D candidates
Research Coordinators
Research Nurses
PACE - MEDPACE CRA...
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...reviews and or audits of the Trial Master File (TMF) to ensure inspection readiness.
~May support clinical monitoring activities, such as CRA training, visit report review, site letters, and escalated site issues.
~May track site qualification, initiation, routine and close...
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Flexibilní pracovní doba
...one or more of the following considered an asset: study start up, regulatory submission, resource management, supervisory experience, CRA, data management, medical writing, or vendor management
~Experience managing dermatology trials
~Experience in SAD-MAD studies is...
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...the Human Data Science Company oriented to drive human health outcomes forward. When you join IQVIA Prague as a sponsor-dedicated CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one...
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...scale project management.
Excellent management, communication, organizational, and problem-solving skills.
Proficiency in Coupa CRA, with technical knowledge.
Expertise in risk management, requirements analysis, change management.
Strong skills in E2E...
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