- CellCarta
- Wilrijk or Antwerp, Belgium (Remote)
- Full-time
Clinical Project Manager
- CellCarta
Wilrijk or Antwerp, Belgium
Full-time
Published:
- CellCarta
Wilrijk or Antwerp, Belgium
Full-time
Published:
Are you looking for an exciting new career opportunity? CellCarta, a Contract Research Organization, is actively seeking a highly skilled and motivated Clinical Project Manager to join our dynamic team. As a Clinical Project Manager, you will have the opportunity to use your expertise and skills to ensure that our services meet the highest industry standards. Come work with a team of talented individuals who are committed to making a positive impact on human health and well-being. Apply today.
SUMMARY:
As a Clinical Project Manager (CPM), you will drive and manage projects with internal stakeholders and external customers (pharma and biotech partners in oncology) to deliver results on time, in full, and in alignment with the CellCarta Quality System.
As a CPM, you will gain a comprehensive understanding of the entire business model and will often be the first to identify what our customers need. As a CPM, you are ultimately responsible for embodying the 3 T’s: keeping the project on Task, on Track, and on Time.
You will need to be comfortable doing the following:
RESPONSIBILITIES:
The CPM is responsible for the delivery of clinical projects within the agreed scope, time, and budget - primarily by coordinating a multitude of tasks performed by internal and external partners. The CPM ensures that each project is executed in compliance with CellCarta’s Quality System. Their responsibilities begin when a clinical project is awarded to CellCarta and conclude once the project is delivered to the sponsor, the study is properly archived, and final invoicing is prepared.
More specifically, you will participate in the following:
EDUCATION:
MAIN REQUIREMENTS:
Essential
Desirable
WHAT WE OFFER
We offer a wide range of benefits including:
ABOUT CELLCARTA:
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The Company operates globally with facilities located in Canada, USA, Belgium, Australia, and China.
Joining CellCarta means working with dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world.
Join us as we make an impact on patient therapy. The information collected to review your application will be processed by the human resources services of CellCarta Biosciences Inc. and its affiliates (collectively, “CellCarta”). The legal basis for this processing is the legitimate interest of CellCarta to evaluate the suitability of candidates for the roles available at CellCarta.
CellCarta will only process that information which is necessary to evaluate your application. This information includes identifying information such as your name, address, email address and phone number, as well as information about your education and professional experience, including previous positions and your CV. Such information is required for us to complete your applicant file, assess your suitability for the role and comply with applicable laws. CellCarta may obtain personal information from other sources, such as during reference, background, or employment checks, with your permission, and from third party sources such as recruitment and assessment sites or professional social media sites, in each case only if such information is relevant to reviewing your application. Your personal information will be retained only for so long as reasonably necessary and in accordance with applicable laws. This information will be processed confidentially and only accessed by those who have a need for the recruitment process. Please note that the information comprising your applicant file may be processed in a country that is not where you are located (for example, you might be in the European Economic Area or Québec, Canada, whereas your applicant file may be reviewed by CellCarta in the United States). If you are offered and accept employment with CellCarta Biosciences Inc. or one of its affiliates, the information collected will become part of your employment record. If you do not want us to retain your information, or want us to update it, please contact privacy@cellcarta.com.
SUMMARY:
As a Clinical Project Manager (CPM), you will drive and manage projects with internal stakeholders and external customers (pharma and biotech partners in oncology) to deliver results on time, in full, and in alignment with the CellCarta Quality System.
As a CPM, you will gain a comprehensive understanding of the entire business model and will often be the first to identify what our customers need. As a CPM, you are ultimately responsible for embodying the 3 T’s: keeping the project on Task, on Track, and on Time.
You will need to be comfortable doing the following:
- Listening actively to the customer and building relationships to ensure client satisfaction;
- Managing yourself effectively under pressure;
- Prioritizing being effective over being right;
- Being open and willing to transform yourself;
- If you are organized, analytically minded, possess a solid technical background, and thrive in a dynamic, high-complexity environment, this might just be the role you’re looking for.
RESPONSIBILITIES:
The CPM is responsible for the delivery of clinical projects within the agreed scope, time, and budget - primarily by coordinating a multitude of tasks performed by internal and external partners. The CPM ensures that each project is executed in compliance with CellCarta’s Quality System. Their responsibilities begin when a clinical project is awarded to CellCarta and conclude once the project is delivered to the sponsor, the study is properly archived, and final invoicing is prepared.
More specifically, you will participate in the following:
- Manage clinical studies from initiation through close-out and archiving, including reporting, in compliance with GCP guidelines and regulations;
- Review all essential documents required for study initiation and ensure audit-ready study files are maintained throughout the duration of the study;
- Prepare and/or approve sample flow designs, study trackers, bioanalytical reports, and other required documentation for clinical studies;
- Monitor and control the study budget;
- Maintain and document professional communication with the sponsor, cross-functional project team, and management throughout the study;
- Chair sponsor calls.
EDUCATION:
- A Master’s degree in Sciences, Biomedical Sciences, Pharmaceutical Sciences, Medical Biology, Medicine, or equivalent expertise gained through experience.
MAIN REQUIREMENTS:
Essential
- 2+ years of project management and/or CRA (Clinical Research Associate) experience, or a background working in histotechnology laboratories;
- A strong curiosity and eagerness to learn, paired with a humble and teachable attitude;
- Proven success in managing complex projects to completion, with positive feedback and the ability to balance multiple priorities effectively;
- Professional-level communication skills; proficient in English, both written and verbal;
- Proficient in Microsoft Office (Word, Excel, PowerPoint, Power BI);
- Excellent organizational skills with the ability to multitask;
- Positive and energetic attitude;
- Self-motivated, adaptable, and able to thrive in a dynamic environment;
- Diligent with strong attention to detail;
- Capable of working both independently and collaboratively;
- Strong critical thinking and problem-solving abilities;
- Customer- and project service–oriented mindset;
- A solution-driven attitude with persistence and determination.
Desirable
- Experience in cancer research, with an understanding of clinical laboratories, assay/instrument principles involved in in vitro diagnostic product design and use, as well as the scientific, statistical, regulatory, and compliance requirements of clinical research;
- Genomics background, with knowledge of key principles, techniques, and platforms;
- Experience working in CAP, CLIA, and GCP environments, with a working knowledge of EMEA and/or FDA guidelines related to clinical trials;
- Experience in data programming and validation;
- Experience working in global settings.
WHAT WE OFFER
We offer a wide range of benefits including:
- A dynamic and rapidly changing global environment that allows for personal growth;
- Training and personal development in a variety of technical and interpersonal areas;
- Career opportunities as the company grows quickly;
- A healthy work-life balance with onsite and remote working;
- A forward-thinking company that is fit for the future;
- A competitive salary and benefits package;
- An excellent team to work with.
ABOUT CELLCARTA:
CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The Company operates globally with facilities located in Canada, USA, Belgium, Australia, and China.
Joining CellCarta means working with dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world.
Join us as we make an impact on patient therapy. The information collected to review your application will be processed by the human resources services of CellCarta Biosciences Inc. and its affiliates (collectively, “CellCarta”). The legal basis for this processing is the legitimate interest of CellCarta to evaluate the suitability of candidates for the roles available at CellCarta.
CellCarta will only process that information which is necessary to evaluate your application. This information includes identifying information such as your name, address, email address and phone number, as well as information about your education and professional experience, including previous positions and your CV. Such information is required for us to complete your applicant file, assess your suitability for the role and comply with applicable laws. CellCarta may obtain personal information from other sources, such as during reference, background, or employment checks, with your permission, and from third party sources such as recruitment and assessment sites or professional social media sites, in each case only if such information is relevant to reviewing your application. Your personal information will be retained only for so long as reasonably necessary and in accordance with applicable laws. This information will be processed confidentially and only accessed by those who have a need for the recruitment process. Please note that the information comprising your applicant file may be processed in a country that is not where you are located (for example, you might be in the European Economic Area or Québec, Canada, whereas your applicant file may be reviewed by CellCarta in the United States). If you are offered and accept employment with CellCarta Biosciences Inc. or one of its affiliates, the information collected will become part of your employment record. If you do not want us to retain your information, or want us to update it, please contact privacy@cellcarta.com.
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