TRABAJO CLINICAL TRIAL MANAGER ONCOLOGY BARCELONA, BARCELONA

Desirable early phase oncology clinical trial experience global study management experience astrazeneca embraces diversity and equality of opportunity...

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

The associate director study leader, early oncology clinical is responsible for the delivery of clinical studies including quality, timelines, budgets, resources...

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... serving as a content manager for study-specific...

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...

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

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

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

Y ou will be adding value through delivering successful support to the project management and clinical trial management groups as well as successfully delivering...

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

clinical input to (s)nda/(s)bla)... possesses detailed knowledge of good clinical practice (gcp) and other regulations governing clinical research...

clinical input to nda/bla)... accountable for the clinical and scientific leadership and integrity of protocols, clinical study reports and/or components of clinical...

• experience in all phases of a clinical study lifecycle... • extensive knowledge of clinical research regulatory requirements (incl ich-gcp) and demonstrated abilities...

Work closely with other intelligence groups within the company (grpi, giace, clinical information science, etc... within oncology regulatory science and strategy...

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

A good understanding of global regulatory requirements for clinical trials and document management and/or experience with clinical trial management systems and patient...

As an associate director in our oncology business unit, you will assist in the creation and implementation of strategies to deliver an exciting and innovative oncology...