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Found 232 jobs in this campaign

Medical information and adverse event intake specialist with german and english language.

IQVIA Safety Operations team play an important part in the design, build and execution of end-to-end safety solutions for major pharmaceutical

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Stage d'Associé de Recherche Clinique - Basé à Paris

L’activité de IQVIA département Sponsor Dédié (FSP) est unique. Nos équipes sont dédiées à un partenaire sponsor unique, dont l’objectif commun

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Experienced Clinical Research Associate, Site Management Poland

Our team is growing, join us on our mission to drive healthcare forward!What We Offer / USPsThe chance to work on cutting edge medicines at the

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Clinical Research Associate - Sponsor dedicated

Clinical Research AssociateIQVIA Turkey is looking for talented and motivated team member to join our Sponsor dedicated team as junior CRA. At

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Feasibility Manager

• Bulgaria, Homeworking
• Competitive

Manager, Feasibility - Remote ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusi

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Senior Clinical Research Associate - FSP (Warsaw/ Łódź/Poznań)

• Poland;Homeworking

If you want to be part of a leading CRO and transform scientific discoveries into new treatments, then Parexel FSP challenges you to live up to you...

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Clinical Site Manager

• Germany, Homeworking
• ICON Strategic Solutions

As Clinical Site Manager you will be responsible for maximizing site performance and site engagement in our client conducted clinical studies, as well

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Digital Recruitment Global Trial Optimization Specialist - Home Based

• United States, Homeworking

As a Digitial Global Trial Optimization Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powere

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Sr Site Contracts Lead

• France; Homeworking
• Syneos Health

Senior Site Contracts Lead Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer succe...

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Clinical Research Associate (m/w/d), Single Sponsor

• Frankfurt/Main

When you join IQVIA as a sponsor-dedicated Clinical Research Associate / CRA (m/w/d) home-based throughout Germany, you’ll enjoy the stability

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Experienced Clinical Research Associate (m/w/d), Multi-Sponsor

Join IQVIA as a CRA / SrCRA (m/w//d) in our Clinical Site Management department home-based throughout Germany. You will focus on a comprehensiv

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Senior Clinical Research Associate (m/w/d), Single Sponsor

Join IQVIA as a Senior Clinical Research Associate / Sr CRA (m/w/d) home-based throughout Germany in our single sponsor department, and advance

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Associate Director/Director - Regulatory Affairs (EMA expert)

• Home-based, United Kingdom

Medpace is the leading CRO for Biotech companies that has continued its growth year-over-year. We are currently seeking a full-time Director / Asso...

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CRA II or Senior CRA - 0.5 FTE (PART-TIME) - Homebased

• Turkey; Homeworking

CRA II or Senior CRA - 0.5 FTE (PART-TIME) - Homebased Sinlge Sponsor Dedicated (FSP) Monitoring experience required as a CRA Syneos Health® is a l...

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Manager, Pharmacovigilance

Pharmacovigilance Manager - Office based (60%) - Bulgaria or Poland ICON plc is a world-leading healthcare intelligence and clinical research organiza

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• United Kingdom, Homeworking

CRA - Multi sponsor (ICON Research Services) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to fo

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• Belgium, Homeworking

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research provid

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Program Manager

• Poland, Homeworking

As a Global Trial Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence

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Clinical Research Associate - Oncology / Multi TA - Chicago, IL

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare in

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• Mexico, Homeworking

CTA - Mexico, Mexico City Hybrid: Office/Remote ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to

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Local Trial Manager (Solid Tumor ONC) - US - Home Based

• Location: United States
• __vacancyopjusttionswidget.opt-Business Area__ ICON Strategic Solutions
• Categories Clinical Trial Management
• __vacancyopjusttionswidget.opt-Remote Working __ Remote

TA Business Partner

• Icon Strategic Solutions

Send me a message

About the role.

As a Local Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

The L-LTM role will be accountable/responsible for ensuring top-quality end-to-end trial delivery at a country level, managing the consistency of Local Trial Management duties and processes.  The L-LTM will serve as the country-level single point of contact on the study for internal partners.  While the L-LTM may delegate tasks to other LTMs or roles on the study, the L-LTM remains accountable for successful completion of those tasks.

The L-LTM will manage and oversee the following throughout the study:

• Central IRB and other local vendors (Greenphire, Drug Destruction services, etc.…) including set up of vendor purchase orders, invoice review and approval, and change-orders, as applicable.
• Execution of local milestones from feasibility through study close out.
• Resourcing of country-level roles, including support with transitions, in collaboration and agreement with the study Functional Manager (FM).
• Inspection Readiness and AQR at the country level.
• Close collaboration with the assigned Local Trial Manager(s) (LTMs), Lead Site Manager (LSM), Site Managers (SMs), Clinical Trial Associates (CTAs), and Site Contract Managers (SCMs) to outline accountabilities/responsibilities and provide support and training, where necessary.
• Efficient communication with the Clinical Trial Managers (CTMs), Clinical Operations and the Global Trial Leader (GTL) to oversee trial excellence.
• Country level ad hoc meetings during any phase of the study that are needed to address unexpected circumstances that might impact country or study level deliverables.
• Close partnership with the study FM to provide updates, discuss hurdles, timelines/resources, and potential risks, and assist with documentation, such as storyboards, lessons-learned, metrics, etc., that may be required by leadership.

What you need to have 

• BA/BS degree.
• Degree in a health or science related field.
• 2 years of local trial management or mutually agreed clinical trial experience.
• Solid tumor oncology trial management experience required
• Specific therapeutic area experience may be required depending on the position.
• Strong working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures.
• Strong IT skills in appropriate software and company systems. Willingness to travel with occasional overnight stay away from home according to business needs.
• Proficient in speaking and writing the country language and English. Good written and oral communication skills as appropriate
• To qualify, applicants must be legally authorized to work in the United States and should not require, now or in the future, sponsorship for employment visa status

What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. https://careers.iconplc.com/reasonable-accommodations Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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