TRABAJO STUDY CANCER CLINICAL TRIALS

Collaborates effectively with study team on study deliverables, as appropriate... contributes to the conduct of study feasibility assessments...

• minimum one year clinical research experience strongly preferred... • assist with periodic review of study files for completeness... • basic knowledge of applicable...

Minimum 4 years’ experience coordinating international clinical trials and managing cros... deep knowledge of international clinical trial regulations (ich-gcp,...

Design, manage, and oversee clinical trial plans, identifying and mitigating risks... global responsibility supervise and guarantee the proper execution and follow...

≥ 2 years of contribution to and accomplishment in all aspects of conducting clinical trials (e... process improvement, training, standard operating procedure (sop)...

Excellent understanding of the clinical study process including monitoring... reports study progress/update to the global study associate director/ global study...

study protocol and patient information sheet, crf, clinical study report, publications etc...     clinical trial main budget control responsible...

≥ 3 years of contribution to and accomplishment in all aspects of conducting clinical trials (e... advanced knowledge and clinical training in a medical/scientific...

Extensive experience in study start-up or clinical operations, with a strong understanding of global regulatory requirements and clinical trial processes...

Implementation of study amendment-and changes in study related processes)... knowledge of clinical trials - knowledge of clinical trial conduct, and skill in applying...

Serve as the medical input to the global development team / subteam and the medical expert for clinical study team development team / subteam and the medical expert...

Day to day responsibilities will include: support clinical research studies and maintain a safe study environment according to health and safety policies under the...

Day to day responsibilities will include: support clinical research studies and maintain a safe study environment according to health and safety policies under...

You’ll gain exposure to various therapeutic areas and clinical study types, creating an excellent foundation for growth in global clinical operations, regulatory...

Experience in executing a wide range of clinical trial activities (from initiation to clinical study report)... develop key study quality metrics (e...

Responsibilities the clinical development medical monitor is part of the clinical department with focus on medical operational aspects related to the clinical...

Your role will involve delivering clinical studies to time, cost, and quality from clinical study protocol (csp) development through to study archiving...

Freelance clinical project manager opportunity position: freelance clinical project managerlocation:- all spain- hybrid (occasional travel when required)contract...

clinical scientist; 5+ years for clinical scientist experience as a clinical scientist support late phase development in the areas of breast and lung cancer...