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Jobs

Clinical Research Documentation Administrator (TMF) Medpace, Inc.

Clinical Research Documentation Administrator (TMF)
Cincinnati, Ohio

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration. Manage electronic filing system for trial documentation; Track, maintain, and perform quality check of electronic documents; Communicate with internal associates globally regarding errors in trial documents; and.

30+ days ago

Clinical Research Associate (Biomedical Engineering Candidates) Medpace Holdings Inc

Clinical Research Associate (Biomedical Engineering Candidates)
Cincinnati, OH

On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

14 days ago
New

Clinical Research Associate (Pharm D Candidates) Medpace Holdings Inc

Clinical Research Associate (Pharm D Candidates)
Cincinnati, OH

On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

2 days ago

Clinical Research Professional I, II or III, Department of Emergency Medicine University of Cincinnati

Clinical Research Professional I, II or III, Department of Emergency Medicine
Cincinnati, OH

Serves as a primary contact for clinical centers in multi-center research studies, develop study materials - serving to train imaging sites, assure study protocol compliance, screen, recruit, and obtain informed consents for clinical trials/studies. Home to more than 53,600 students, 12,000 faculty and staff, and over 360,000 living alumni, UC, a Carnegie 1 institution, combines research prowess with a physical setting The New York Times has called "the most ambitious campus design program in the country."

9 days ago

Clinical Research Documentation Administrator (TMF) Medpace Holdings Inc

Clinical Research Documentation Administrator (TMF)
Cincinnati, OH

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration. Manage electronic filing system for trial documentation; Track, maintain, and perform quality check of electronic documents; Communicate with internal associates globally regarding errors in trial documents; and.

30+ days ago

Clinical Nurse Study Coordinator Medpace, Inc.

Clinical Nurse Study Coordinator
Cincinnati, Ohio

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. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

30+ days ago

Senior Clinical Research Associate (level dependent on experience) CTI

Senior Clinical Research Associate (level dependent on experience)
Covington, Kentucky
Remote

For that reason, we treat our team members with the respect they deserve, and our numbers show it: We support career progression – We believe in promoting from within and we have a structured mentoring program and program for recent graduates to provide the support employees need to move forward. To help support the unique job functions of our CRAs, we have a dedicated training department that offers ongoing therapeutic training sessions from our world-class medical directors, and an experienced and supportive management team that is there to offer continual guidance.

30+ days ago

Clinical Project Coordinator Medpace, Inc.

Clinical Project Coordinator
Cincinnati, Ohio

Responsibilities: Provide day-to-day departmental/project support activities, such as maintenance of project-related files and and IRB document preparation and submissions; Data entry into Medpace proprietary systems and Excel spreadsheets; Coordinate and provide minutes for department/project meetings or conference calls; Maintain spreadsheets and compile reports; and. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

18 days ago

Clinical Project Coordinator Medpace Holdings Inc

Clinical Project Coordinator
Cincinnati, OH

Provide day-to-day departmental/project support activities, such as maintenance of project-related files and and IRB document preparation and submissions; Data entry into Medpace proprietary systems and Excel spreadsheets; Coordinate and provide minutes for department/project meetings or conference calls; Maintain spreadsheets and compile reports; and. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

17 days ago

Clinical Research RN - MOB Lindner Research HV - Full Time - Days The Christ Hospital Health Network

Clinical Research RN - MOB Lindner Research HV - Full Time - Days
Cincinnati, OH

Assists in project initiation, which includes educating physicians and hospital staff, implementing study protocol assignments, facilitating patient enrollment and follow-up. Encourages new patient enrollment by identifying potential research patients, discussing the protocols with physicians and communicating this information to the screeners to facilitate the process.

16 days ago

Clinical Research Nurse-RN - MOB Linder Research HV - Full Time - Days The Christ Hospital Health Network

Clinical Research Nurse-RN - MOB Linder Research HV - Full Time - Days
Cincinnati, OH

Assists in project initiation, which includes educating physicians and hospital staff, implementing study protocol assignments, facilitating patient enrollment and follow-up. Encourages new patient enrollment by identifying potential research patients, discussing the protocols with physicians and communicating this information to the screeners to facilitate the process.

8 days ago

Clinical Research Nurse TriHealth Inc

Clinical Research Nurse
Cincinnati, OH

Acts as a liaison between Study Sponsors, Study Monitors, Principal Investigators, other physicians, hospital staff, and the Institutional Review Board (IRB) to coordinate the efforts necessary to efficiently and effectively conduct a clinical research study. Actively participate in the selection of studies TriHealth conducts, developing a process for implementation of the protocol, participating in the identification of potential subjects, participating in the informed consent process, enrolling subjects and accurately and thoroughly collecting and reporting data.

30+ days ago

Clinical Research Nurse-RN - MOB Linder Research HV - Full Time - Days The Christ Hospital

Clinical Research Nurse-RN - MOB Linder Research HV - Full Time - Days
Cincinnati, OH

Assists in project initiation, which includes educating physicians and hospital staff, implementing study protocol assignments, facilitating patient enrollment and follow-up. Encourages new patient enrollment by identifying potential research patients, discussing the protocols with physicians and communicating this information to the screeners to facilitate the process.

7 days ago
New

Clinical Research Coordinator II/III - Bone Marrow Transplantation Cincinnati Children's Hospital Medical Center

Clinical Research Coordinator II/III - Bone Marrow Transplantation
Cincinnati, OH

Serve as CCHMC liaison to internal departments, clinical teams, regulatory agencies, physician's offices, city clinics, government agencies, academic centers, and other organizations. Recruitment/Enrollment/Retention - Determine best method/s to identify potential participants for research protocol (advertisements, chart reviews, monitoring of clinic schedule, etc.) and prepare accordingly.

4 days ago
Thermo Fisher Scientific logo

Project Manager, Central Labs Thermo Fisher Scientific

Project Manager, Central Labs
Highland Heights, Kentucky
Remote

Guide and support workflow of Project Managers and Set-up Administrators with special attention to training junior personnel, perform as a mentor and trainer for (newly assigned) Project Managers, identify areas for development and efficiencies in performing tasks, author, review, revise and implement relevant procedural documents, and serve as a backup for the Associate Director PM when needed. The Project Manager, Central Labs monitors and manages all aspects of designated clinical trial protocols in Global Central Labs and is accountable for overall project performance and client’s satisfaction by meeting their needs and expectations through the life cycle of the assigned clinical trials.

7 days ago

Study Start-Up Project Manager Medpace, Inc.

Study Start-Up Project Manager
Cincinnati, Ohio

Effectively lead others in a matrix environment; Perform quality checks on submission documents and site essential documents; Prepare and approve informed consent forms; Serve as a Sponsor point of contact for start-up and regulatory submissions items; Review pertinent regulations to develop proactive solutions to start-up challenges; Prepare new business proposals and present during bid defenses, general capabilities meetings, and audits; Contribute to the growth and development of departmental staff, processes and systems. Qualifications: Bachelor's degree required, advanced degree in Life Sciences preferred; 5+ years of experience in clinical research, preferably at a CRO in Study Start-Up or as a Research Manager at a study site; Project management experience and demonstrated role in developing others; and.

14 days ago

Finance Account Manager Medpace, Inc.

Finance Account Manager
Cincinnati, Ohio

Qualifications: Bachelor's degree in business, finance, or accounting; 5 years of experience in the conduct of clinical research and/or contract management/pricing; Strong working knowledge of financial and accounting processes; Basic knowledge of medical terminology and working knowledge of drug development services; Excellent analytical, as well as written and oral communication, skills; Excellent computer skills with a strong knowledge of Excel; and. Responsibilities: Prepare and follow through on bids for new business; Oversee financial and contractual performance of Sponsor projects; Maintain a strong relationship with the customer during an ongoing clinical trial; Perform financial analysis and reporting; Oversee client requests for proposals; Develop change-in-scope documents for ongoing trials; Customize pricing according to client requirements; Develop study metrics; and.

30+ days ago

eClinical Project Manager Medpace, Inc.

eClinical Project Manager
Cincinnati, Ohio

Qualifications: Bachelor’s degree and prior eClinical experience; including setting up and managing multiple eClinical/eCOA projects and acting as the main point of contact for the sponsor; General knowledge of technology trends and system / application development; Possess excellent organizational, prioritization, and time management skills; A basic knowledge of medical terminology is needed, as well as knowledge of a scientific investigative methodologies and clinical research methodologies. Responsibilities: Manage multiple projects from am eClinincal/eCOA perspective; Develop and review study documentation related to eClinical/eCOA activities for clinical trials with sponsor companies and other departments; Coordinate overall eClinical activities by serving as primary contact for the sponsor; Monitor study timelines in relation to clinical trial needs; Attend face to face sponsor meetings and Investigator Meetings.

29 days ago

Feasibility Manager Medpace, Inc.

Feasibility Manager
Cincinnati, Ohio

Conduct feasibility assessments for strategic or high priority clients in support of proposal development for new business opportunities, and provide high quality, accurate feasibility data to internal and external teams; Present feasibility results to members of the proposal team to ensure correct assumptions were applied and strategy is in line with our therapeutic and operational experience; As needed to support feasibility strategy, coordinate outreach to investigative sites to obtain indication and protocol specific feedback; Provide management, mentoring, training and guidance to more junior members of the team, including entry level feasibility coordinators; Work collaboratively with project teams to support preparation for proposal documents and bid defense meetings; and. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

30+ days ago

Project Finance Account Manager Medpace, Inc.

Project Finance Account Manager
Cincinnati, Ohio

Qualifications: Bachelor's degree in business, finance, or accounting; 5 years of experience in the conduct of clinical research and/or contract management/pricing; Strong working knowledge of financial and accounting processes; Basic knowledge of medical terminology and working knowledge of drug development services; Excellent analytical, as well as written and oral communication, skills; Excellent computer skills with a strong knowledge of Microsoft® Excel; and. Responsibilities: Prepare and follow through on bids for new business; Oversee financial and contractual performance of Sponsor projects; Maintain a strong relationship with the customer during an ongoing clinical trial; Perform financial analysis and reporting; Oversee client requests for proposals; Develop change-in-scope documents for ongoing trials; Customize pricing according to client requirements; Develop study metrics; and.

30+ days ago
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