Company: Docs Global (Continental Europe)
Reference: Ref AS-020148
Closing Date: 20 Jan 17
Salary (£): Competitive
Benefits: Excellent & Comprehensive
We are looking for talented and motivated candidates to join the team and take part in this long term, dynamic project within an internationational Pharmaceutical Company.
Roles & Responsibilities of the position
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
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
Must be able to travel in accordance with company and project requirements
We offer a permanent contract, full time and partially home based in Milan, Rome, Bologna or Florence.
For an immediate consideration please send your most recent resume directly 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, Integrity, Openness.
CRO, Pharma, Pharmaceutical, Biotechnology, Biotech, Clinical Research Organisation, Medical Device, Permanent, Full time, Clinical Research, Clinical Trial, Associate, Project Management, Senior, Manager, Career, Clinical Research Associates, CRA, SCRA, Clinical Monitoring, Site Monitor, Site Manager, CPM, Clinical Trial Manager, Therapeutic Areas, Indication, Oncology, Respiratory, Cardiovascular, cardiology, Rheumatology, Diabetes, Ophthalmology, Dermatology, Urology, CNS, Neurology, hematology, orphan diseases, nephrology, musculoskeletal, endocrinology, gastroenterology, Recruitment.
2 Globeside, Globeside Business Park
|Website:||Visit Our Web Site|
PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.