Clinical Research Coordinator

Celerion; Lincoln (NE); On-site; USD 50,000 - 70,000; Full time

Job summary

Celerion in Lincoln, NE is seeking a Clinical Research Coordinator to oversee and conduct clinical studies, ensuring compliance and quality. This is ideal for someone seeking a career change with provided training. You will manage studies from initiation to execution, solve problems during the process, and build relationships with clients.

The role requires a Bachelor’s degree or BSN, along with skills in organization, communication, and customer service. Celerion values integrity, trust, teamwork, and respect.

Qualifications

• Bachelor’s degree in a related discipline or BSN required.
• Industry experience and knowledge of medical terminology preferred.
• Demonstrated organizational, time management and multi-tasking skills required.
• Excellent oral and written communication skills required.

Responsibilities

• Oversee and conduct clinical studies ensuring compliance, quality, and profitability.
• Manage overall Clinical Studies including performance and execution.
• Build client relationships and respond to client issues.

Skills

Organizational skills

Time management

Excellent oral and written communication skills

Customer service skills

Ability to work flexible hours

Education

Bachelor’s degree in a related discipline or BSN

Job description

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.

We are seeking a Clinical Research Coordinator to join our Lincoln, NE team! This is a great opportunity for someone seeking a career change. Training is provided.

As a Clinical Research Coordinator 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 this role you should plan to work some evening and weekends.

Primary Responsibilities

You are responsible for the overall management of Clinical Studies to include: on-time performance with defect-free execution, independently conducting bioequivalency and bioavailability studies, working with support divisions to ensure timelines are being met in clinical studies (i.e. recruiting, data management, statistics), organizing study initiation meetings to plan execution of study, facilitating study review meetings for pre-study, in-process and post study review, problem solving as needed during study conduct, meeting with clients as needed throughout study, and organizing study logistics and personnel. In addition, you will be present at critical events and dosings of study. You will build client relationships that result in additional business, you will craft and edit reports, respond to client issues, concerns and requests, adhere to milestone guidelines, and ensure profitability by maintaining profitability of team through a budgeting and expense control on a total and individual study basis.

Requirements

• You will have a Bachelor’s degree in a related discipline or BSN required. Celerion experience may be considered in lieu of degree in some situations.
• Industry experience and knowledge of medical terminology preferred.
• Demonstrated organizational, time management and multi-tasking skills required.
• Shown ability to handle multiple priorities.
• Excellent oral and written communication skills.
• You will work without close supervision.
• Ability to work flexible hours required for study conduct.
• You will utilize customer service skills.
• Clinical Research experience useful, but not required.

Celerion Values: Integrity Trust Teamwork Respect

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.