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Principal Investigator
Summary:
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Celerion is a global organisation offering one of the most experienced clinical pharmacologyEmployment Type: Full-Time
Catering Specialist (Casual)
Summary:
Catering Specialist Every member of the Celerion team is involved in making something essential – a distinctive contribution to the health and well-being of people around the world. That’s the sense of purpose shared by employees throughout Celerion. We’re an early phase drug research company, opeEmployment Type: Full-Time
Consumer Study Coordinator (30 hrs/wk) - Richmond, Virginia
Summary:
Celerion is currently seeking a Consumer Study Coordinator at our Richmond, VA location. Our Richmond location focuses on consumer opinion studies related to nicotine and tobacco products. This position will work 30 hours per week and is eligible for benefits. We are looking for someone who has theEmployment Type: Part-Time, Benefited
Salary: 19 - 19 USD per-hour-wage
Clinical Data Specialist (part time)
Summary:
The Clinical Data Specialist is responsible for the review of all source data and ensure all applicable data is entered into its respective database and/or Case Report Form (CRF). Ensure the completeness, accuracy, and consistency of source data and CRF data entry so that it meets the standard of quEmployment Type: Variable / Casual
Remote
Director, Global Training and Development
Summary:
Build Something from Scratch. Empower Global Teams. Drive Learning Innovation. Are you a builder, strategist, and hands-on leader who thrives on creating systems and programs that help global teams excel? If so, let's talk! Celerion is seeking a Director, Global Training and Development to design aEmployment Type: Full-Time
Bioanalytical Principal Investigator - Ligand Binding
Summary:
Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you! Location: Corporate office in Lincoln, NE. Just south of downtown. As a Bioanalytical Principal Investigator, you will have overall responsibility for the technical conduct oEmployment Type: Full-Time
Production Nurse
Summary:
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Celerion is committed to swift, exceptional clinical research through translational medicineEmployment Type: Full-Time
Clinical Data Specialist
Summary:
The Clinical Data Specialist is responsible for the review of all source data and ensure all applicable data is entered into its respective database and/or Case Report Form (CRF). Ensure the completeness, accuracy, and consistency of source data and CRF data entry so that it meets the standard of quEmployment Type: Full-Time
Remote
EDC Test Analyst
Summary:
As an EDC Test Analyst, you will serve as the critical link between database design and successful execution. You will validate clinical databases and systems that support clinical research, ensuring every study launches according to specifications. Working in collaboration with Clinical Data ManagEmployment Type: Full-Time
Remote
EDC Developer / Programmer
Summary:
Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you! We are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Electronic Data Capture (EDC) DataEmployment Type: Full-Time
Clinical Data Specialist
Summary:
Responsible for the review of all source data and ensure all applicable data is entered into its respective database and/or Case Report Form (CRF). Ensure the completeness, accuracy, and consistency of source data and CRF data entry so that it meets the standard of quality expected for reporting toEmployment Type: Full-Time
Salary: 19.5 - 21.5 USD per-hour-wage
Remote
Scientific Report Associate
Summary:
Scientific Report Associate Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Celerion offers one of the most experienced clinical pharmacEmployment Type: Full-Time
Remote
Trial Master File Representative (Remote - UK)
Summary:
TMF Representative Join a team that's going places! Every member of Celerion is involved in making a distinctive contribution to the health and well-being of people around the world. That's the sense of purpose shared by our employees. We are a performance-driven drug research company, operating inEmployment Type: Full-Time
Scientific Report Associate - Lincoln, Nebraska
Summary:
Celerion is searching for a full-time Scientific Report Associate for our Lincoln, NE location. This position will generate, template, and format preliminary and final Clinical Study Reports. This position will build appendices, import information from various sources and format the report per clienEmployment Type: Full-Time
Automation Specialist 100%
Summary:
Celerion is one of the world's leading bioanalytical contract research organizations and has been supporting pharmaceutical and biotech drug development programs around the world for more than 40 years. Due to the steady growth of our company and to strengthen our bioanalytical laboratory in the LEmployment Type: Part-Time, Benefited
Remote
Trial Master Files Representative
Summary:
Celerion, a leader in the clinical research industry, currently has an opportunity for a Full-Time Trial Master Files Representative to join our team. This is a remote, home-based position and may be filled from any US geography. In this position, you will be be involved in the preparation and thEmployment Type: Full-Time
Salary: 24 - 29 USD per-hour-wage
Scientist LC-MS 100%
Summary:
Celerion is one of the world's leading bioanalytical contract research organizations and has been supporting pharmaceutical and biotech drug development programs around the world for more than 40 years. Due to the steady growth of our company and to strengthen our bioanalytical laboratory in FehralEmployment Type: Full-Time
Research Nurse
Summary:
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Celerion offers one of the most experienced clinical pharmacology research networks in theEmployment Type: Full-Time
Call Center Representative (2nd Shift - Mon-Fri 11:30am-8:00pm) - Richmond, Virginia area
Summary:
Celerion is currently seeking a Call Center Representative to join our Glen Allen, Virginia team! Do you enjoy providing excellent customer service? If so, we may have the position for you! We have a Part-time benefitted position available that will work 30-35 hours per week. In this role, you wilEmployment Type: Full-Time
Salary: 18 - 18 USD per-hour-wage
Remote
Clinical Project Coordinator (Part-Time)
Summary:
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Are you looking for an opportunity that will make a difference in the future of healthcare?Employment Type: Variable / Casual
Clinical Conduct Specialist
Summary:
Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you! We have an exciting opportunity to become a Clinical Conduct Specialist in our Tempe clinic! In this position you will be assisting Clinical Study Managers with study preparaEmployment Type: Full-Time
Salary: 21 - 21 USD per-hour-wage
Clinical Study Manager I
Summary:
As a Clinical Study Manager you are responsible for oversight and conduct of clinical studies. You will ensure compliance, quality, and profitability of clinical studies. You respond to internal and external client issues, concerns, and requests by applying study management techniques and tools. In