Trial Manager

6 maanden geleden

Groningen, Nederland Charles River Laboratories Voltijd

**Req ID #**:223165**Location**:Groningen, NL- For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.- What describes you best? A energetic scientist in Neuroscience or other Life Sciences with a hands on mentality? Can you translate your scientific approach to the customer? Is this you then this is your moment_
- To join our team at Charles River Laboratories at our site in Groningen we are looking for a dedicated_

**Trial Manager/ Study Director**

**Our site**:
With 27 employees our site is a dedicated group focusing on non-GLP DMPK (drug metabolism and pharmacokinetics) and pharmacology studies to better understand neuroscience disease pathophysiology. including but not limited to, micro dialysis, electrophysiology, rapid pharmacokinetic screening and bioanalysis.

**The team**:
As we are a small site who support our clients drug discovery programs. We work individually and in tight conjunction with scientific staff and animal technicians. You have a lot of interaction with your colleagues, and all are happy to jump in and help where needed.
**Your roll**:
As a Trial Manager/ Study Director you will be responsible for each research project from the moment the study is signed, until report delivery and completion. This includes study design and planning, evaluation of results, communication of potential challenges and proposed resolutions and presenting results to our clients. As part of the study management team, you will be discussing interesting findings with your colleagues, and work together to identify resolutions when facing challenges during a study.

**Responsibilities**:

- Monitoring validity and scientific quality of your studies; performing quality checks of ongoing studies;
- Advising clients on most appropriate study designs and testing strategies, and building a trust-based relationship with returning clients;
- Depending on your personal interests and existing competencies you can also be an partner in regulatory

**Qualifications**:

- Advanced academic degree (MSc of higher) in Neuroscience or other Life Sciences;
- Understanding of neuroscience on the cellular and systems level ;
- Fluent English oral and written ;
- Pro-active, results oriented:

- Excellent communication, interpersonal and teamwork abilities, and positive attitude.

**Nice to have**:

- Article 9 (Laboratory Animal Science);
- Industry experience.

**Our offer**:
Working at our organization means working in a dynamic international organization. In addition, we offer excellent primary and secondary working conditions including:

- 25 vacation days
- Possibility to purchase 10 additional vacation days per year;
- Annual one-time 8% vacation pay of your gross annual salary;
- Annual one-time payment based on company results;
- Travel allowance at € 0.21 cents per kilometer with a maximum of € 225 net per month,
- Collective Aegon Capitall pension with a personal contribution of 2.9%;
- Collective health insurance with CZ or VGZ. 10 to 12% discount on any supplementary insurance.

Do you have any questions about this vacancy?
For further information about the position, please contact Maaike Verrijt at**Acquisition in response to this vacancy is not appreciated**

**About Discovery**About Charles River**
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.- At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.**

  • Trial Manager

    5 maanden geleden

    Groningen, Nederland Charles River Voltijd

    For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will...

  • Clinical Safety Manager

    3 maanden geleden

    Groningen, Nederland QPS Voltijd

    **QPS Netherlands B.V. in Groningen **is part of an international organization and conducts drug research on behalf of international pharmaceutical and biotechnological companies. We are seeking an experienced **Clinical Safety Manager** to lead and oversee the Safety Management process within clinical trials. In this role, you will be responsible for...

  • Clinical Safety Manager

    3 maanden geleden

    Groningen, Nederland QPS Voltijd

    QPS Netherlands B.V. in Groningen is part of an international organization and conducts drug research on behalf of international pharmaceutical and biotechnological companies. We are seeking an experienced Clinical Safety Manager to lead and oversee the Safety Management process within clinical trials. In this role, you will be responsible for establishing...

  • Clinical Safety Manager

    1 maand geleden

    Groningen, Nederland QPS, LLC Voltijd

    **Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you!** QPS is seeking an experienced **Clinical Safety Manager** to lead the safety team and oversee the Safety Management process within clinical trials. In this role, you will be responsible for establishing...

  • Clinical Study Manager II

    2 maanden geleden

    Groningen, Groningen, Nederland Icon plc Voltijd

    Clinical Study Manager II Job SummaryAt ICON plc, we're proud to foster an inclusive environment driving innovation and excellence. We're seeking a Clinical Study Manager II to provide clinical trial management for in-house and outsourced studies. Reviews and assesses research protocols, clinic budgets, case report forms, informed consent forms, and study...

  • Clinical Safety Manager

    3 maanden geleden

    Groningen, Nederland QPS, LLC Voltijd

    **Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you!** QPS is seeking an experienced **Clinical Safety Manager** to lead and oversee the Safety Management process within clinical trials. In this role, you will be responsible for establishing safety reporting...

  • Clinical Study Manager Ii

    2 maanden geleden

    Groningen, Nederland Icon plc Voltijd

    Clinical Study Manager - Phase I Research ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development The Clinical Study Manager II provides clinical trial...

  • Clinical Research Coordinator

    4 maanden geleden

    Groningen, Nederland IQVIA Voltijd

    Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Clinical Research Coordinator to support a site in Groningen. As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support the clinical trial team and ensure the smooth running of the clinical...

  • Clinical Research Coordinator

    6 maanden geleden

    Groningen, Nederland IQVIA Voltijd

    Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Clinical Research Coordinator to support a site in Groningen. As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support the clinical trial team and ensure the smooth running of the clinical...

  • Clinical Research Coordinator

    3 weken geleden

    Groningen, Nederland IQVIA Voltijd

    Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Clinical Research Coordinator to support a site in Groningen. This role is for 21 **hours **per week and is expected to last approximately until beginning of April 2025. As a pivotal member of the site team, you will be involved with a variety...

  • Clinical Safety Manager

    1 maand geleden

    Groningen, Nederland QPS Voltijd

    Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! QPS is seeking an experienced Clinical Safety Manager to lead the safety team and oversee the Safety Management process within clinical trials. In this role, you will be responsible for establishing...

  • Clinical Research Coordinator

    7 maanden geleden

    Groningen, Nederland IQVIA Voltijd

    Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Clinical Research Coordinator to support a site in Groningen. This freelance role is for 21 hours per week and is expected to last approximately 12-17 months. The successful candidate will be responsible for supporting a clinical research...

  • Clinical Study Manager II- Fixed-term contract

    7 maanden geleden

    Groningen, Nederland PRA Voltijd

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...

  • Clinical Research Coordinator

    2 weken geleden

    Groningen, Groningen, Nederland Icon plc Voltijd

    About ICON plcICON plc is a world-leading healthcare intelligence and clinical research organization. We foster an inclusive environment driving innovation and excellence, welcoming talented individuals to join our mission shaping the future of clinical development.Job OverviewThe Clinical Study Manager II oversees clinical trial management for in-house and...

  • Teamleider Servicedesk Clinical Research Office

    2 maanden geleden

    Groningen, Nederland UMCG Voltijd

    **Functiebeschrijving**: Als teamleider bij Servicedesk Clinical Research Office (SD CRO) ben je de spil in de coördinatie en bedrijfsvoering. Je fungeert als het aanspreekpunt voor zowel medewerkers als stakeholders en zorgt voor een evenwichtige balans tussen ondernemerschap en dienstverlenende activiteiten: - je stuurt 15 medewerkers van de SD CRO en 2...

  • Clinical Study Manager II

    7 maanden geleden

    Groningen, Nederland PRA Voltijd

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...