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Job Details

Site Manager LD

Company: Docs Global (Continental Europe)
Location: Italy
Reference: Ref AS-019383
Closing Date: 10 Dec 16
Type: Contract
Salary (£): Competitive
Benefits: Excellent & Comprehensive

Job Summary:

We are looking for talented and motivated CRAs to join the team and take part in this long term, dynamic project within an international Pharmaceutical company!

Requirements:

Roles & Responsibilities of the position

The CRA II or SR CRA is responsible for the support and management of study sites for Phase II- IV clinical studies according to SOP’s, GCP regulations and protocol requirements.
Identify, evaluate and recommend potential study sites for participation based on feasibility
Perform pre-trial assessment visits and coordinate site initiation visits
Assures that site personnel complete and document protocol-specific training
Conducts on-going study visits and perform Monitoring visits on a routine basis
Performs source documentation as required by SOP to ensure protocol/patient compliance
Reports any site issues to Clinical Team
Ensures that Trial Centre File (TCF) is current up to date
Performs drug accountability and any re-labelling that may be required
Responds to site questions and escalates as necessary for resolution
Attends investigator meetings
Participate in QA or FDA audits when necessary

Job Requirements

Education: BSN/BS/MS or BA required
Experience: a minimum of two years Clinical Research experience
Knowledge of Microsoft Office applications especially Excel
English: Fluent spoken & written
Good interpersonal skills demonstrated as proactive, enthusiastic, and independent thinker
Ability to collaborate and build strong relationships with all functions involved in the trial
Works and meets deadlines with some supervision

Remuneration & other details

We offer a permanent contract, full time and home based in Milan, Rome, Bologna, Florence or Naples.

To apply:
For an immediate consideration please send your most recent resume to vera.stellino@docsglobal.com. This is an excellent opportunity that should not be missed, don’t miss out and apply today!

About DOCS:
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.

Key words:
CRO, Pharma, Pharmaceutical, Biotechnology, Biotech, Clinical Research Organisation, Medical Device, Permanent, Full-time, Clinical Research, Associate, Project Management, Senior, Manager, Career, Clinical Research Associates, CRA, SCRA, Clinical Monitoring, Site Monitor, Site Manager, CPM, Clinical Trial Manager, Study Director, Project Leader, Non-interventional, Therapeutic Areas, Indication, Oncology, Respiratory, Cardiovascular, cardiology, Rheumatology, Diabetes, Ophthalmology, Dermatology, Urology, CNS, Neurology

Apply for this job: Site Manager LD

Contact Information:

Address:  Head Office
2 Globeside, Globeside Business Park
Marlow
Buckinghamshire
SL7 1HZ
England
Website:  Visit Our Web Site

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