![Icon plc](https://media.trabajo.org/img/noimg.jpg)
Cra Ii/ Senior Cra
vor 2 Monaten
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 our customers and help us to fulfil our mission to advance and improve patients’ lives.
Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.
As a Clinical Research Associate at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP.
The role:
- Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
- Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions
- Balancing sponsor generated queries
- Taking responsibility for study cost efficiency
- Preparation and review of study documentation and feasibility studies for new proposals
- Potential to assist in training and mentoring fellow CRAs
You will need:
- 18 months+ of monitoring experience in phase I-III trials as a CRA
- College degree in medicine, science, or equivalent
- Previous monitoring experience in medium-sized studies, including study start-up and close-out
- Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
- Excellent written and verbal communication
- Ability to work to tight deadlines
- Availability to travel least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license
Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON 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.
LI-JC3
LI-Remote
-
Cra Ii
vor 2 Monaten
Frankfurt am Main, Deutschland Warman O'Brien VollzeitA global CRO is looking to hire experienced CRAs (CRA II or Senior CRAs) to join them on a permanent basis in Germany. Working across therapeutic areas, and covering the full life-cycle of clinical trials, the CRA will be responsible for the preparation, initiation, monitoring and closure of assigned sites in clinical studies in phase II-IV, in compliance...
-
CRA II
vor 2 Wochen
Frankfurt am Main, Deutschland Proclinical Staffing VollzeitCRA II / SCRA - Global Pharma Salary: Highly Competitive Job type: Permanent Discipline: Clinical Research Associate (CRA) Location: ...
-
CRA II
vor 3 Wochen
Frankfurt, Deutschland Proclinical VollzeitProclinical is seeking a CRA II / SCRA to join a reputable Global Pharma company. The successful candidate will be expected to travel to sites frequently, demonstrating excellent communication skills and a strong understanding of ICH-GCP guidelines. Responsibilities:Monitoring and overseeing medium-sized studies from start-up to close-outReviewing and...
-
CRA II
vor 2 Wochen
Frankfurt, Deutschland Pharmiweb VollzeitProclinical is seeking a CRA II / SCRA to join a reputable Global Pharma company in Germany. The successful candidate will be expected to travel to sites frequently, demonstrating excellent communication skills and a strong understanding of ICH-GCP guidelines. Responsibilities:Monitoring and overseeing medium-sized studies from start-up to close-outReviewing...
-
CRA II
vor 3 Wochen
Frankfurt, Deutschland Pharmiweb VollzeitProclinical is seeking a CRA II / SCRA to join a reputable Global Pharma company. The successful candidate will be expected to travel to sites frequently, demonstrating excellent communication skills and a strong understanding of ICH-GCP guidelines. Responsibilities:Monitoring and overseeing medium-sized studies from start-up to close-outReviewing and...
-
CRA II
vor 2 Wochen
Frankfurt, Deutschland Proclinical Staffing VollzeitProclinical is seeking a CRA II / SCRA to join a reputable Global Pharma company in Germany. The successful candidate will be expected to travel to sites frequently, demonstrating excellent communication skills and a strong understanding of ICH-GCP guidelines. Responsibilities:Monitoring and overseeing medium-sized studies from start-up to close-outReviewing...
-
Clinical Research Associate or Senior Cra
vor 2 Monaten
Frankfurt am Main, Deutschland Novasyte VollzeitWe are looking for an experienced CRA or Senior CRA (m/w/d) for a sponsor dedicated role in cooperation with Boehringer Ingelheim, one of the largest and most established pharmaceutical companies in Germany (family owned since 1885), with focus on therapeutic areas such as Pulmonology, Oncology and Neurology. When you join the IQVIA sponsor-dedicated cFSP...
-
Cra or Senior Cra
vor 2 Monaten
Frankfurt am Main, Deutschland Novasyte VollzeitAre you interested in supporting our pharma clients with conducting clinical trials in different therapeutic areas? Join IQVIA as a CRA/SrCRA (m/w//d) in our Clinical Site Management department office-based in Frankfurt or home-based throughout Germany. You will focus on a comprehensive clinical trial management in a variety of indications and learn about...
-
Cra or Senior Cra
vor 2 Monaten
Frankfurt am Main, Deutschland Novasyte VollzeitAre you interested in collaborating with leading pharma companies to help patients all around the world?- When you join IQVIA as a sponsor-dedicated CRA/SrCRA (m/w/d) office-based in Frankfurt or home-based throughout Germany, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with...
-
Cra Trainee
vor 2 Monaten
Frankfurt am Main, Deutschland Novasyte VollzeitJoin IQVIA as CRA Trainee / Associate CRA (m/w/d) in the sponsor dedicated team and work in home-office throughout Germany. In our _Clinical Functional Service Partnership_ models, we work in a close partnership with key customers to deliver a comprehensive clinical trial management. Within this team, you will focus on different projects of one single...
-
CRA II
vor 2 Wochen
Frankfurt, Deutschland Pharmiweb VollzeitProclinical is seeking multiple CRAs to join a reputable Clinical Research Organisation in Germany. The successful candidate will work as part of a vast team and a fast-paced environment alongside a dedicated team to select, initiate and close-out investigational sites for clinical studies in phases I - IV, ensuring adherence to applicable regulations and...
-
Cra Ii
vor 1 Monat
Frankfurt am Main, Deutschland Ergomed VollzeitCompany Description Ergomed PLC is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease. Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia Our company allows for employee visibility (you...
-
Wertpapierrecht Volljurist:in
vor 2 Monaten
Frankfurt am Main, Deutschland Flex Suisse GmbH VollzeitFlex Suisse ist ein alternativer Rechtsdienstleister und führender Anbieter von Legal & Compliance Services in Deutschland, Schweiz, Liechtenstein und Singapur. Zu unseren Partnern gehören führende Wirtschaftskanzleien, Großbanken und Industriekonzerne. Für unseren Kunden, eine internationale Ratingagentur, suchen wir ab sofort eine: n Volljurist: in...
-
Scientist Ii
vor 3 Monaten
Ludwigshafen am Rhein, Deutschland AbbVie Vollzeit**Company Description** **Job Description** Gemeinsam Großes bewegen - mit einer Karriere, die Dich inspiriert **Gemeinsam Großes bewegen - mit einer Karriere, in der Du mehr erreichen kannst** Herzlich willkommen bei Abbvie! Als Teil eines internationalen Unternehmens mit über 48.000 Mitarbeitern weltweit und rund 3.000 Mitarbeitern in Deutschland hast...
-
Clinical Research Associate, sponsor dedicated
vor 2 Monaten
Frankfurt, Deutschland Pharmiweb VollzeitThe 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...
-
Senior Actuarial Consultant
Vor 3 Tagen
Frankfurt am Main, Hessen, Deutschland Mazars GmbH & Co. KG VollzeitJob Overview:As a Senior Actuarial Consultant, you will play a pivotal role in guiding our clients in the insurance sector through various critical projects.Key Responsibilities:Oversee subprojects focused on advising insurance firms in enhancing their processes, validating models, and ensuring compliance with Solvency II and IFRS 17 standards.Conduct...
-
Senior Actuarial Consultant
vor 14 Stunden
Frankfurt am Main, Hessen, Deutschland Mazars GmbH & Co. KG VollzeitJob Overview:As a Senior Actuarial Consultant, you will take the lead on various subprojects aimed at enhancing the operational efficiency of insurance firms. Your expertise will be crucial in areas such as model validation, Solvency II compliance, and IFRS 17 standards.Key Responsibilities:Oversee subprojects focused on advising insurance organizations...
-
Senior Actuarial Consultant
vor 14 Stunden
Frankfurt am Main, Hessen, Deutschland Mazars GmbH & Co. KG VollzeitJob Overview:As a Senior Actuarial Consultant, you will play a pivotal role in enhancing our consulting services for insurance firms. Your responsibilities will include:Leading Subprojects: Oversee initiatives focused on advising insurance organizations on process enhancement, model assessment, and compliance with Solvency II and IFRS 17 standards.Cash Flow...
-
Senior Actuarial Consultant
Vor 3 Tagen
Frankfurt am Main, Hessen, Deutschland Mazars GmbH & Co. KG VollzeitJob Overview:As a Senior Actuarial Consultant, you will play a pivotal role in enhancing our consulting services for insurance firms. Your responsibilities will include:Leading subprojects focused on advising insurance companies regarding process enhancement, model validation, and compliance with Solvency II and IFRS 17 standards.Conducting thorough analyses...
-
Senior Consultant Insurance
vor 3 Monaten
Frankfurt am Main, Hessen, Deutschland Deloitte Germany VollzeitSenior Consultant Insurance / Financial Services (m/w/d) Du willst im Bereich Audit & Assurance – Insurance die Qualität und den Mehrwert unserer Prüfungen sicherstellen? Unser Team befasst sich mit reinen Prüfungsthemen, mit Neuerungen im Aufsichtsrecht und mit Best Practices des Risikomanagements und Accounting in der Versicherungsbranche. Sichere...