Clinical Trial Manager
1 settimana fa
Parexel is currently seeking a Global Clinical Trial Manager (CTM) to join us in Italy, dedicated to a single sponsor.This role will act as a member of the sponsor's Development Operations team.The Clinical Trials Manager will manage individual clinical trials and/or programs as part of the Clinical Trial Working Group.Working as a Clinical Trial Manager at Parexel FSP offers tremendous long-term job security and prospects.We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50.And we have an incredible pipeline of work.Expect exciting professional challenges in inspiring studies, but with time for your outside life.ResponsibilitiesManage external vendors and contract research organizationsPrepare study documents such as the Monitoring Manual, Study Operations Manual, Source Data Verification Plan and Laboratory ManualCoordinate and be responsible for the design of study materials such as CRFs, patient diaries, study participation cards and source documentsAssist with protocol development and study report completionManage monitoring activities (may include routine on-site clinical monitoring) at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs and study protocolsProvide guidance, direction, and management to CRAsTrack patient enrollment; qualify, initiate, monitor, perform closeout activities, and review site reports; and assist in coordination of data management activitiesCoordinate study suppliesNegotiate contracts with vendors of clinical trial servicesRequirementsBachelor's, nursing degree or equivalent required, science preferred.5 or more years of industry experience in global clinical studies (Pharmaceutical, Biotech or CRO).Proven track record with relevant clinical trials experience, including strong performance as a CRA in the pharmaceutical industry (i.e. biotechnology, pharmaceutical, CRO, medical device).Proven experience of clinical trial management.Experience in CNS and / or oncology is preferred.Proven management/leadership of people in a matrixed environment.Management of global clinical trials.Demonstrated working knowledge of GCP, ICH guidelines and FDA regulations.Demonstrated ability to work independently and in a team environment.Travel required.Must be willing to travel *****%, including international travel.Proficiency with MS Office (e.g. Word, Excel, PowerPoint, Outlook).Excellent oral and written communication skills and strong organisational abilities.We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers.In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel.Who are ParexelParexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.We supported the trials of most of today's top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.You'll be an influential member of the wider team.Not quite the role for you?Join Our Talent Community and we'll reach out with job alerts when positions that match your career interests become available.We'll also share periodic updates about the latest company news and events.Sign up today
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Clinical Trial Manager
1 settimana fa
Lazio, Italia Advanced Clinical A tempo pienoClinical Trial Manager – Italy | Advanced Clinical (FSP Model) Oncology focusedAdvanced Clinical is seeking an experienced Clinical Trial Manager to join our UK-based Functional Service Provider (FSP) team.This role will support global clinical studies and requires strong operational, vendor management, and monitoring oversight...
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Clinical Trial Manager
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Lazio, Italia Altro A tempo pienoClinical Trial Manager – RomeJoin to apply for the Clinical Trial Manager role at Bristol Myers Squibb .About the RoleThe Clinical Trial Manager (CTM) is accountable for end-to-end study operational oversight and delivery at country level (Italy, Greece, Israel and Croatia), ensuring adherence to timelines, budget and quality standards.Acts as the primary...
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Clinical Trial Manager
1 settimana fa
Lazio, Italia Parexel International A tempo pienoParexel is currently seeking a Global Clinical Trial Manager (CTM) to join us in Italy, dedicated to a single sponsor.This role will act as a member of the sponsor's Development Operations team.The Clinical Trials Manager will manage individual clinical trials and/or programs as part of the Clinical Trial Working Group.Working as a Clinical Trial Manager at...
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Sponsor-Dedicated Clinical Trial Manager
5 giorni fa
Lazio, Italia Qit Iqvia Rds Italy S.R.L. A tempo pienoA leading clinical research company in Rome is seeking a Clinical Trial Manager to ensure the successful delivery of clinical studies, particularly in the oncology area.The role requires a Bachelor's Degree in Life Sciences and at least 1 year of clinical trial management experience.Strong leadership, effective communication, and organizational skills are...
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Clinical Trial Manager
7 giorni fa
Lazio, Italia Altro A tempo pienoClinical Trial Manager – Rome Join to apply for theClinical Trial Managerrole atBristol Myers Squibb .About the RoleTheClinical Trial Manager (CTM)is accountable for end-to-end study operational oversight and delivery at country level (Italy, Greece, Israel and Croatia), ensuring adherence to timelines, budget and quality standards.Acts as the primary...
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Clinical Trial Documentation
5 giorni fa
Lazio, Italia Chiesi Group A tempo pienoClinical Trial Documentation & Records Management Lead Join to apply for the Clinical Trial Documentation & Records Management Lead role at Chiesi GroupBased in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with 90 years' experience, operating in 31 countries with more than 7,000 employees (Chiesi Group).To...
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Clinical Trial Documentation
3 giorni fa
Lazio, Italia Chiesi Group A tempo pienoClinical Trial Documentation & Records Management LeadJoin to apply for the Clinical Trial Documentation & Records Management Lead role at Chiesi GroupBased in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with 90 years' experience, operating in 31 countries with more than 7,000 employees (Chiesi Group). To...
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Clinical Trial Docs
5 giorni fa
Lazio, Italia Chiesi Group A tempo pienoA global pharmaceutical company based in Parma, Italy is seeking a Clinical Trial Documentation & Records Management Lead.This role requires leadership in managing clinical documentation and records, ensuring compliance with regulatory standards, and overseeing clinical trial technologies.Candidates should have 8-10 years of experience in clinical operations...
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Clinical Trial Manager
2 settimane fa
Lazio, Italia Iqvia Llc A tempo pienoClinical Project Manager - based in Rome (Sponsor dedicated) page is loaded## Clinical Project Manager - based in Rome (Sponsor dedicated)locations: Rome, Roma, Italytime type: Full timeposted on: Posted Todayjob requisition id: R The **IQVIA Clinical Functional Service Partnerships (Clinical FSP)** department is providing highly skilled professionals to our...
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Clinical Trial Manager
1 giorno fa
Lazio, Italia Altro A tempo pienoClinical Project Manager – Based in Rome (Sponsor dedicated)The IQVIA Clinical Functional Service Partnerships (Clinical FSP) department provides highly skilled professionals to client project teams to set up and execute clinical trials. This role works on diverse therapeutic areas.Clinical Project Manager is an integral part of trial delivery, liaising...
