Clinical Nurse Study Coordinator

Medpace; Cincinnati (OH); Hybrid; USD 60,000 - 80,000; Full time

Benefits offered by this job

Hybrid work-from-home options

Competitive PTO packages, starting at 20+ days

Flexible work hours

Discounted tuition for UC online programs

Company-sponsored employee appreciation events

Health and wellness initiatives

Job summary

A biopharmaceutical company is seeking a full-time Study Coordinator to join their Clinical Pharmacology Unit in Cincinnati, Ohio. This role involves working on a team to manage study subjects, ensure safe medication administration, and assess adverse events. Candidates should have a Bachelor's degree and a nursing license (RN) along with clinical experience in an acute care setting. The company offers hybrid work options and numerous benefits including competitive PTO, career development opportunities, and a modern office environment.

Qualifications

• Bachelor's degree required, preferably in nursing.
• Clinical experience in an acute care setting is preferred.

Responsibilities

• Assist in interviewing and evaluating prospective study subjects.
• Responsible for administering medications according to protocols.
• Assess subjects for adverse events and document them.
• Perform and schedule procedures such as vital signs and laboratory tests.
• Work closely with Project Managers on operational matters.
• Interact with study Monitors and resolve data queries.

Skills

Clinical experience in acute care setting

Education

Bachelor's degree

Nursing license (RN)

Job description

Job Summary

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Study Coordinator to join our Clinical Pharmacology Unit 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 use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities

• May assist in interviewing, evaluating, and scheduling prospective study subjects according to protocol criteria;
• Responsible for accurate and safe administration of medications according to protocols;
• Responsible for assessing subjects for adverse events and ensuring they are documented;
• Perform and/or schedule procedures (e.g. vital signs, intravenous insertions, venipunctures, laboratory tests, ECGs, etc.);
• Work closely with Project Managers on operational matters (i.e. study execution planning, operational flow);
• Interacts with study Monitors and resolving data queries, confirming eligible subjects, and interacting with the Investigator for medical matters.

Qualifications

• Bachelor's degree, nursing license (RN);
• Clinical experience in acute care setting preferred.

Benefits

• Cincinnati Campus Overview
• Hybrid work-from-home options (dependent upon position and level)
• Competitive PTO packages, starting at 20+ days
• Flexible work hours
• Discounted tuition for UC online programs
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
• Community involvement with local nonprofit organizations
• Competitive compensation and benefits package
• Structured career paths with opportunities for professional growth
• Partnership and discount with onsite childcare
• Discounts on local sports games, local fitness gyms and attractions
  • Official Sponsor of FC Cincinnati
• Modern, ecofriendly campus with an on-site fitness center, bar, and restaurants

EO/AA Employer M/F/Disability/Vets