Clinical Project Coordinator

Il y a 5 mois


Leuven, Belgique Medpace, Inc. Temps plein

Job Summary:
Medpace Reference Laboratories is a global, full-service central clinical trial laboratory specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio, USA and we are active in over 80 countries across the globe. Medpace has established laboratories in the USA, Europe, Singapore, and China. Our services continue to expand, with the introduction of new laboratory capabilities in all our global laboratories.

Medpace Reference Laboratories is a full service central clinical trial laboratory offering project management, laboratory services, data management, logistics, and sample management and archiving capabilities, and quality assurance. Medpace Reference Laboratories (MRL) is currently seeking a full-time Project Coordinator.

Responsibilities:

- Maintain study-related documents;
- Attending study team calls;
- Primary point of contact for study teams and investigational sites;
- Preparing study metrics;
- Ensure that all aspects of designated clinical protocol are in accordance with project timelines, budgets and performance quality;
- Coordinate laboratory shipments;
- Compose and maintain departmental operating procedures and work instructions; and
- Interact with Project Managers, Sponsors, and vendors on project-related issues.

Qualifications:

- Min. Bachelor's degree in life sciences (e.g. Biomedical Sciences)
- Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills.

Medpace Overview:
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?:
When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.

**Awards**:

- Medpace historically named a Top Cincinnati Workplace by the Cincinnati Enquirer
- Recognized by Forbes as one of America's Best Mid-size Companies in 2021
- Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availability
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
- Ranked in the top 10 on the 2021 LinkedIn Top Companies list in Cincinnati

**What to Expect Next**:
A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an interview.
- EO/AA Employer M/F/Disability/Vets_


  • Project Coordinator

    il y a 2 semaines


    Leuven, Belgique Medpace, Inc. Temps plein

    Job Summary: Medpace Reference Laboratories is a global, full-service central clinical trial laboratory specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio, USA and we are active in over 80 countries across the globe. Medpace has established laboratories in the USA, Europe, Singapore, and China. Our services...


  • Leuven, Belgique Medpace, Inc. Temps plein

    Job Summary: Responsibilities: - Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager - Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy - Compile and maintain project-specific status reports within the clinical trial management system - Interact...


  • Leuven, Belgique Medpace, Inc. Temps plein

    Job Summary: Responsibilities: - Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager - Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy - Compile and maintain project-specific status reports within the clinical trial management system - Interact...


  • Leuven, Belgique PSI CRO Temps plein

    Company Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 1,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...

  • Clinical Trial Manager

    il y a 5 jours


    Leuven, Belgique Medpace, Inc. Temps plein

    Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Leuven, Belgium. Clinical Trial Managers with expertise in Nephrology are welcome to continue to work in their area of expertise or to expand to a new therapeutic area....

  • Data Coordinator

    il y a 1 mois


    Leuven, Belgique Medpace, Inc. Temps plein

    Job Summary: Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Data Coordinator for our Medpace Reference Laboratories to join our Data Management team in Leuven, Belgium. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. By analysing...


  • Leuven, Belgique Meet Recruitment Temps plein

    50000 EUR - 50000 EUR - Leuven, Belgium - Permanent **Study Start Up & Regulatory Coordinator - Global CRO - Hybrid - Leuven, Belgium** I am currently working alongside my client, a global CRO with a long and rich history within Clinical Research, to support them in their search for a Study Start Up & Regulatory Submissions Coordinator to join their...


  • Leuven, Belgique Terumo Europe NV Temps plein

    Taken en verantwoordelijkheden The main responsibility of the Project Coordinator Digital Experience is to support and coordinate Digital Projects within the realm of the Digital Experience Team within the Terumo Interventional Systems department. The Project Coordinator Digital Experience collaborates with the Communication and Brand Experience team to...

  • Fleet Coordinator

    Il y a 6 mois


    Leuven, Belgique MEDPACE Temps plein

    Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We...

  • Fleet Coordinator

    Il y a 6 mois


    Leuven, Belgique Medpace, Inc. Temps plein

    Job Summary: We are seeking a full-time, office-based Fleet Coordinator to join our team in Leuven within a permanent contract. If you want an exciting career where you use your previous expertise in Facilities and have a strong desire to develop and grow your career even further, then this is the opportunity for you. Responsibilities: - The Fleet...


  • Leuven, Belgique Medpace, Inc. Temps plein

    Job Summary: Our global business is growing rapidly, and we are currently seeking a full-time office-based Clinical Database Programmer to join our Data Management team in our Leuven office. This position will work in a team to develop databases in which clinical data are captured and processed for analysis and reporting. The role requires the ability to...


  • Leuven, Belgique Innovative Trials Temps plein

    **Start Date**: Mid/End November **FTE**: 0.2 **Location**: Belgium **Job Purpose** The Clinical Enrolment Manager (CEM) will perform site optimisation services in order to boost patient recruitment for clients’ clinical trials. The site optimisation services include, but are not limited to: Site Optimisation Calls - the telephone-based coaching of...


  • Leuven, Belgique Flamingo Therapeutics Temps plein

    **About us** Flamingo is pioneering RNA-targeted therapies for oncology with a clinical-stage pipeline targeting undruggable transcription factors and long non-coding RNAs. **Role and key responsibilities**: - Assist in defining the project scope and objectives, involving relevant stakeholders; - Provide comprehensive oversight and management of vendors,...


  • Leuven, Belgique Medpace, Inc. Temps plein

    Job Summary: Our global business is growing rapidly, and we are currently seeking a full-time, office-based Clinical Database Programmer to join our Data Management team in our Leuven office. The position will work in a team to develop databases in which clinical data are captured and processed for analysis and reporting. This position plays a critical role...


  • Leuven, Belgique Flamingo Therapeutics Temps plein

    **About us** Flamingo is pioneering RNA-targeted therapies for oncology with a clinical-stage pipeline targeting undruggable transcription factors and long non-coding RNAs. **Role and key responsibilities**: - Assist in defining the project scope and objectives, involving relevant stakeholders; - Provide comprehensive oversight and management of vendors,...


  • Leuven, Belgique Stryker Corporation Temps plein

    **The Job’s mission**: **Have you always wanted to work for one of the world's best employers within medical technology and an award-winning Great Place to Work Belgium?** For our innovative Mako robotics system, we are looking for a **Hybrid** **Clinical (Mako) Support Specialist** to cover the regions of **Antwerpen, Vlaams-Brabant & Limburg **in...

  • Project Manager

    Il y a 7 mois


    Leuven, Belgique Septentrio Temps plein

    **For our Leuven offices, we are looking for highly qualified and motivated professionals like you. If you think you have what it takes to keep Septentrio firmly in Pole Position, get in touch.** **We need you for the position of** **Project Manager** **The Job** Our Project Manager has a crucial role in our R&D organization, is responsible for several...


  • Leuven, Belgique KU Leuven Temps plein

    Msc in data science-adjacent fields (biostatistics, bioinformatics, computer science, bioengineering, biotechnology).Background:Implementation, training and benchmarking of deep neural networks (PyTorch experience is a plus) .Experience in molecular biology is a plusExperience in single-cell transcriptomics analysis is a plusExperience with communication to...


  • Leuven, Belgique Medpace, Inc. Temps plein

    Job Summary: Our clinical activities are growing rapidly, and we are currently seeking a full-time Regulatory Submissions Coordinator (Study Start Up Specialist) to join our Clinical Operations team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you...

  • Sales Coordinator

    Il y a 5 mois


    Leuven, Belgique Sterigenics Temps plein

    The Sales Coordinator is responsible for the support of the commercial organization as it relates to presales and post-sales activities which aligns our commercial activities with the corporate mission. This position will liaise with account managers and strategic account directors for qualifying leads, establishing new customers in the system, coordinating...