LAVORO CLINICAL MONITOR MEDICAL DEVICE

clinical trial management support, data management, submission dossier, clinical study reports, etc... ) previous experience in medical writing/reading...

Product knowledge including product vigilance and medical device reporting... working knowledge of clinical research, good clinical practice (gcp) and regulatory...

Job overview the medical department consists of a chief medical officer, medical directors, sr medical directors, medical writers, and safety associates...

clinical activities... provides medical review of ecrfs for clinical accuracy... job overview the medical department consists of a chief medical officer, medical...

Deep understanding of local regulatory policy and industry’s code of practice related to drug registration, pharmaceutical promotion and clinical study is preferred...

What to expect? reporting to the associate director medical affairs emea, the medical science liaison northern europe will manage the regional efforts of the medical...

They are looking for a clinical affairs program manager europe... as part of the global clinical affairs team, you will be responsible for developing strategies...

By collaborating with clinical core team members, this role ensures that clinical data management activities are executed consistently and in compliance with regulatory...

Regional surgical clinical manager (m/f/d) germany south & central as the regional surgical clinical manager, you will have the exciting opportunity to lead a dynamic...

Pricing and reimbursement dossiers, heor dossiers, medical information packs, clinical expert reviews etc... monitor the environment for competitive intelligence...

At least five (5) years of experience advising on r&d clinical legal issues, such as clinical trial design, and working understanding of laws and regulations impacting...

clinical research certification (acrp or socra, clinical coordinator/cra certification) preferred... experience working in a medical device or regulated industry...

Experience with medical device clinical trials... clinical trial experience required (sponsor or cro)... intimate knowledge of good clinical practices (gcp) and...

Operational experience in clinical development with significant direct exposure to implementation of novel approaches in clinical development...

Cro, central labs) and investigators perform medical monitoring of clinical trial data work cross-sector in pharmaceutical and/or medical device spaces qualifications...