TRABAJO CLINICAL TRIAL BARCELONA, BARCELONA

This is what you will do: assist the cpls for the planning, implementation, execution and compliance of operational plans for clinical study/program with multiple...

You will need to have: 2 years of clinical research experience or course-work equivalent in clinical research... you will be responsible for: ensuring clinical study...

clinical input to nda/bla)... prepare and provide input to clinical study reports (csrs) and clinical portions of regulatory documents (e...

Typical responsibilities may include: •    provide long-range clinical planning in early clinical trial development, planning and managing of clinical research projects...

Understanding of scientific and clinical issues related to the design and implementation of clinical trials and interpreting trial results particularly in respiratory...

Engage with clinical investigators on clinical studies to enable quality clinical execution, analyze and interpret clinical data, and collaborate with the broader...

The clinical research medical advisor is a global clinical development role with medical responsibility for the clinical trial process...

Assist in the clinical trial insurance process; track approvals, revisions and renewals of certificates... lead the preparation of country specific agreements, confidentiality...

• oversee the clinical trial insurance process; track approvals, revisions and renewals of certificates... • lead the preparation of country specific agreements...

Provides matrix management of functional area representatives to cross functional clinical study teams... the associate director study leader, early oncology clinical...

Crfs, diary cards, lab supplies, drug supplies, and study binders) as appropriate   • *to assist project teams with trial progress tracking by updating the clinical...

Extensive knowledge of all steps included in a clinical trial... training / strong knowledge on good clinical practices... experience: 2-3 years of experience in...

• performs site initiation visit, ensures site personnel is fully trained on all trial related aspects... • proactively collaborates with the site & study operations...

The project manager, trial interactive (pm) is the main point of contact for clients at transperfect interactive throughout assigned projects and relationships...

clinical input to (s)nda/(s)bla)... implement clinical r&d policies, sops and related directives... they share responsibility with clinical operations team members...