Ref #: 25644

Employment type: Permanent - Full-Time

Location: Poland - home-based

Posted: 30-Jan-2021

Description

DOCS Global, an FSP Division of ICON Clinical, are working with a Global Biopharmaceutical company in building a large FSP team within a global clinical operations in Poland.

We are looking for experienced Global Project Managers/Study Managers /Global Trial Managers to join our newly established global study management team.


How to apply:

Please contact Dariusz Sternlicht, Recruitment Consultant at DOCS on +48 606 130 397 or email your up-to-date CV to: dariusz.sternlicht@docsglobal.com



Responsibilities include:

The Global Study Manager (GSM) is responsible for the operational planning, management & execution of clinical study.

The GSM is the leader of the clinical study team and empowered to drive the management & delivery of the study team operational objectives , ensuring all trial deliverables are met according to the study timelines, within budget and having the highest quality standards (GCP / ICH, SOPs / QDs).

Leads the preparation of study related plans and materials, identification of study risks and contingency planning, appropriate escalation of issues, monitors the study planning, manages budget to ensure it is kept within budget and leads the execution of the study with integrity and suitable for regulatory review.

Leads cross-functional study teams: responsible for the coordination of internal/ external resources, organization of internal team meetings, s/he drives and oversees vendors for the flawless execution of studies.

Responsible for management of Clinical and Medical Service Providers, set up & oversight of service providers and ensure adherence to scope of work within timelines and budget.


Requirements:

Bachelor or Master in (Bio)Medical Sciences, Chemistry, Pharmacology, Life Sciences or related study.
Solid Project Management background
Solid experience of oversight on activities covering all study periods from start-up to study report
Experience of working at a CRO or a pharmaceutical company
Vendor management experience
Demonstrated ability to work well both on a cross-functional team and independently
Leadership/project management skills


If you are seeking an international company who is committed to development and training and the opportunity for career progression, please get in contact.

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