TRABAJO SAFETY MANAGER CLINICAL TRIALS

Ability to work on multiple trials in parallel... sr local trial manager position summary: a senior, local trial manager is a mid-level trial management role with...

clinical trials expertise:   utilize your background in clinical trials to lead value-based special projects... clinical trials experience:   minimum of 3-5 years...

Prepares and/or reviews regulatory documents to support clinical trial submissions... responsibilities acts as a clinical trial regulatory manager (ctrm) on complex...

Originated in switzerland, psi is a privately owned, full-service cro with a global reach, supporting clinical trials across multiple countries and continents...

They are looking for a clinical affairs program manager europe... additional responsibilities include management of clinical trials approvals with local irbs and/or...

The clinical safety specialist is responsible for implementing and executing clinical trial safety activities and responsibilities for the clinical research programs...

Skills: clinical trials... experience in preparing or contributing to the preparation of clinical safety assessments and regulatory reports/submissions involving...

clinical project manager reports to the director, clinical affairs and will manage the operational acti viti es for assigned abiomed clinical study(ies)...

Experience with medical device clinical trials... intimate knowledge of good clinical practices (gcp) and iso guidelines for governing the conduct of clinical trials...

We are currently looking to hire a clinical pharmacology department manager... job requirementsbachelor of medicinespecialist in clinical pharmacologyenglish, high...

Knowledge of clinical trials - knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i...

Johnson & johnson is currently seeking an analyst ii, clinical data manager... knowledge of applicable international guidelines regarding data management of clinical...

Participate in monitoring study safety... able to manage complex and/or large trials... experience in executing a wide range of clinical trial activities (from initiation...

Knowledge and experience of non-interventional studies (nis), registry studies, phase iv clinical trials or pass/paes... demonstrated in-depth knowledge of study...

The manager, medical writing will oversee post-market surveillance activities within the clinical and regulatory affairs department... primary duties and responsibilities:...

Experience: •    minimum 3+ years of experience in pharmacovigilance, working on clinical studies and/or study safety methodology... job description: •    collaborate...

Job description actual position name: clinical data scientist reporting to the clinical data science manager, the clinical data scientist is an integral part of...