Company: Docs Global (Continental Europe)
Reference: Ref AS-019289
Closing Date: 24 Jan 17
Salary (£): Competitive
Benefits: Excellent & Comprehensive
DOCS has partnered with a highly prestigious organization with one of the most robust pipeline within the industry. This is a fantastic opportunity for an experienced clinical research professional that is ready to take on a new challenge as Medical Affairs Operations Trial Manager, based in Italy-Milan.
Roles & Responsibilities of the position
The Medical Affairs Operations Trial Manager is accountable for leading with success the execution of local company data generation activities in one or more countries for project(s) assigned by the Clinical Program Leader, Functional Manager, or Clinical Operations Head.
This includes all project activities starting from Request for Services and high level budget estimate through protocol development to delivery of final Clinical Study report (CSR) or other deliverable(s), according to planned milestones, within budget, and with high quality standards per company procedures and regulatory requirements
For projects executed in-house, the Trial Manager will oversee and support CRAs and other team members in the daily operational activities in line with country specific regulations and internal processes, if required.
For projects outsourced to a CRO, the Trial Manager will oversee and monitor the CRO’s performance on all contracted services.
Monitors patient recruitment rate to ensure that target enrollment will be met across the allocated regions/countries and escalates issues and manages risks related to resources, timelines and budgets
Bachelor’s degree or equivalent required, preferably in Life Sciences (e.g. Biology, Chemistry, Biochemistry, Nursing, Pharmacy).
Minimum of 5 years of clinical trial experience in the pharmaceutical industry or CRO.
Clinical operations knowledge, project management and proficient communication skills are required.
Excellent decision-making and strong financial management skills are essential for this position.
Effective study team leadership skills and proven ability to foster team productivity and cohesiveness.
Flexibility and ability to manage study teams in a virtual environment are needed.
Ability to work on multiple projects in parallel in different therapeutic areas is required.
Experience in managing all study types mainly non-interventional.
This is a permanent role, full time and client office based!
For an immediate consideration please send your most recent resume to firstname.lastname@example.org
DOCS has grown to become the premier resourcing provider of global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997 we are driven by our core values that guide our culture and support our goal to become a Trusted Partner. Our five core values are: Our People, Excellence, Accountability, and Integrity.
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2 Globeside, Globeside Business Park
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