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Senior clinical research associate - contractor - germany - home based.

• Berlin, Germany
• Competitive
• Worldwide Clinical Trials

Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology

View details Senior Clinical Research Associate - Contractor - Germany - Home based

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• Germany, Homeworking
• ICON Strategic Solutions

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovat

View details CRA II

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Senior Clinical Research Associate - Germany - Home based

View details Senior Clinical Research Associate - Germany - Home based

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Experienced Clinical Research Associate

• Munich, Germany

Our clinical activities are growing rapidly, and we are currently seeking an Experienced Clinical Research Associate to join our Clinical Operation...

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Junior Clinical Research Associate

The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device...

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CRA II/ Senior CRA

CRA II or Senior CRA Homebased across Germany At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to ou

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Clinical Research Associate (w/m/d), sponsor-dedicated (w/m/d) - Home Office, Deutschland

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortre...

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Clinical Research Associate, sponsor dedicated

The Clinical Research Associate will perform site activities for Phase I-IV studies operating as the main point of contact for the site during a study

View details Clinical Research Associate, sponsor dedicated

• 11 days ago
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Experienced Clinical Research Associate (m/w/d), Multi-Sponsor

• Frankfurt/Main

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

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

• 15 days ago
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Clinical Research Associate (m/w/d), Single Sponsor

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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Clinical Research Pharma Jobs in Europe

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Find jobs in clinical research, clinical trials, CROs, Pharmacovigilance and Medical Information , and Regulatory Affairs . Find a job as a Clinical Research Associate (CRA) or Clinical Research Manager.

Clinical Research jobs in Austria (2) , Belgium (4) , Bulgaria (1) , Denmark (2) , France (4) , Germany (11) , Hungary (4) , Ireland (3) , Malta (1) , Multiple Countries (10) , Netherlands (1) , Poland (3) , Portugal (1) , Spain (2) , Sweden (2) , Switzerland (1) and United Kingdom (8) .

Associate Director Clinical Medical Affairs

The Associate Clinical Affairs Medical Director will serve key roles to provide leadership on medical, scientific, and clinical decisions to meet growing need for medical expertise...

Product Development Manager - Drug/Device Combination Products

Lead the Design Control process for drug/device combination products and create phase-based Design Control documents (DDP, URS, DRS, DV&V, DTx, DHF, etc.). Determine the...

Medical Director

Ensure appropriate affiliate resourcing, skills and capabilities are in place to support affiliate, regional and global medical affairs activities, global research, and development...

Medical Director - Contrast Media & Molecular Imaging

You will lead the clinical development strategy and be responsible for designing and executing clinical development plans for MR Imaging assigned contrast agents...

Medical Director, Oncology

You will provide therapeutic and drug development expertise and interact with Sponsors and investigative sites on protocol medical issues. Contribute to investigator meeting...

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Senior Regulatory Manager - Regulatory Affairs Medtech

Monitor and analyze the impact of emerging or revised laws, regulations, enforcement actions and other changes that impact the manner by which the clients' products are regulated...

Associate Director/Director, Regulatory

This role serves as a close business partner and facilitator of regulatory activities and is expected to contribute to developing sound regulatory strategies globally. The role...

Sr. Specialist Regulatory Affairs

Create and Review regulatory documentation for Drug, Device and Combination product renewals with major focus on Medical Device renewals; Track status and progress of regulatory...

Clinical Project Manager

Ensuring clinical studies are conducted according to the study protocol, SOPs, ICH/GCP regulations, and study-specific manuals and procedures; Participating in the development of...

Senior Medical Writer

Senior specialist, regulatory affairs, manager regulatory cmc strategy, senior project manager - early phase esource, scientist target identification and selection, clinical research physician, senior staff regulatory affairs specialist, data analyst - corporate drug safety, global patient scientist, rare diseases - cdd, good clinical practice (gcp) senior quality assurance (qa) oversight, clinical research scientist - mi, nm, & pet, senior quality process specialist, associate director - regulatory affairs, senior director, inflammation ta global safety leader, clinical lead ii/iii, regulatory affairs & compliance manager - dental implant system, clinical development lead, medical advisor oncology, drug regulatory team leader, development project lead, lead clinical studies and logistics, senior biostatistician, principal/statistical programmer analyst/consultant, senior specialist regulatory affairs - nordics, senior statistical programmer analyst/consultant, director regulatory affairs oncology, director - medical writer, senior regional medical advisor, uk and ireland, regulatory affairs specialist, cmc specialist, senior safety scientist, pharmacovigilance associate, sr. medical science liaison - rare disease, quality assurance officer, associate ra specialist, post market, freelance clinical research associate, regulatory affairs coordinator, senior clinical trial manager, medical science liaison, senior statistical programmer - eu, pharmacovigilance associate - data surveillance, clinical trial associate, global regulatory affairs manager, managing consultant, designing innovative clinical trial designs, principal biostatistician, regulatory affairs specialist - medical devices, global site management lead, medical/clinical advisor, manager, risk management implementation, director regulatory affairs, don't forget to mention europharmajobs when applying., free job alerts.

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Clinical Research Associate - Sponsor Dedicated - Germany

• Location: Germany
• Categories Clinical Monitoring
• __vacancyopjusttionswidget.opt-Business Area__ ICON Strategic Solutions
• __vacancyopjusttionswidget.opt-Remote Working __ Remote

TA Business Partner

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About the role, this vacancy has now expired. please see similar roles below....

As a Clinical Reserach Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. The Clinical Research Associate will perform site activities for Phase I-IV studies operating as the main point of contact for the site during a study. Drive and execute monitoring plans, ensure site GCP compliance, write trip reports, resolve issues and facilitate open issue resolution, work on recruitment strategies, and monitor safety at the site.  The CRA  will conduct site qualification visits as assigned, site initiation visits and site training, routine monitoring visits, and site close-out visits. Perform investigator site management activities in adherence to all applicable regulatory guidelines and standard operating procedures (SOPs).

The Clinical Research Associate is ultimately responsible for the successful management of investigator sites and monitoring activities for assigned clinical studies throughout the trial lifecycle. Key responsibilities include:

• Full ownership of investigator sites for assigned studies, with responsibility for the successful management of the site right through to close-out, in accordance with the clinical monitoring plan.
• Developing effective relationships with investigator site staff (at sites in Southern Germany and Switzerland) to ensure that key clinical metrics are met.
• Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and working diligently to relevant guidelines.

To enable success in this position you will have:

• At least 1.5 years as an independent CRA, including conducting monitoring visits for clinical trials, from either a pharmaceutical company or a CRO environment.
• A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential.
• You will be educated to degree level in a life science discipline or be a licensed healthcare professional.
• Fluency in German and English is essential
• Scientific degree (BSc, MSc or PhD), have equivalent experience or be a licensed healthcare professional.

Benefits of Working in ICON: Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development. At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future. ICON, including subsidiaries, is an equal opportunity and inclusive employer and 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.

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To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her

Brazil-based CRA II Debora Oh shares her tips on how to become a great CRA and provides insight into life at ICON.

How to progress as a Clinical Research AssociateTo thrive as a Clinical Research Associate (CRA), it is imperative to cultivate a multifaceted skill set and demonstrate unwavering commitment to exce

 Senior CRA Yemi Moses recounts her development and shares her career ambitions with ICON plc.

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Senior Clinical Research Associate, Suzaita Hipolito, talks about how working in Clinical Research gives her happiness and fulfilment.

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