Job Summary Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Coordinator to join our Data Management team. This position involves ...
Job Summary Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Coordinator to join our Data Management team. This position involves ...
Clinical Data Manager
San Diego, CA · On-site
$110K - $120K/yr
The Clinical Data Manager will ensure timely conduct of Clinical Data Management activities for assigned studies according to protocols, industry standards and guidelines, Standard Operating ...
Clinical Data Manager
San Diego, CA · On-site
$110K - $120K/yr
The Clinical Data Manager will ensure timely conduct of Clinical Data Management activities for assigned studies according to protocols, industry standards and guidelines, Standard Operating ...
Clinical Data Managers
Campus, IL · On-site
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Manage all data management activities of a clinical trial in the maintenance phase of the project.
Clinical Data Managers
Campus, IL · On-site
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Manage all data management activities of a clinical trial in the maintenance phase of the project.
Clinical Data Managers
Salt Lake City, UT · On-site
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Manage all data management activities of a clinical trial in the maintenance phase of the project.
Clinical Data Managers
Salt Lake City, UT · On-site
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Manage all data management activities of a clinical trial in the maintenance phase of the project.
Clinical Data Managers
Campus, IL · On-site
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Manage all data management activities of a clinical trial in the maintenance phase of the project.
Clinical Data Managers
Campus, IL · On-site
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Manage all data management activities of a clinical trial in the maintenance phase of the project.
Clinical Data Managers
Campus, IL · On-site
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Manage all data management activities of a clinical trial in the maintenance phase of the project.
Clinical Data Managers
Campus, IL · On-site
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Manage all data management activities of a clinical trial in the maintenance phase of the project.
Clinical Data Managers
Salt Lake City, UT · On-site
$54K/yr
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Manage all data management activities of a clinical trial in the maintenance phase of the project.
Clinical Data Managers
Salt Lake City, UT · On-site
$54K/yr
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Manage all data management activities of a clinical trial in the maintenance phase of the project.
Clinical Data Managers
Salt Lake City, UT · On-site
$39K - $54K/yr
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Responsibilities Clinical Data Manager, II Develop data management plans that deliver accurate ...
Clinical Data Managers
Salt Lake City, UT · On-site
$39K - $54K/yr
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Responsibilities Clinical Data Manager, II Develop data management plans that deliver accurate ...
Clinical Data Managers
Campus, IL · On-site
$39K - $54K/yr
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Responsibilities Clinical Data Manager, II Develop data management plans that deliver accurate ...
Clinical Data Managers
Campus, IL · On-site
$39K - $54K/yr
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Responsibilities Clinical Data Manager, II Develop data management plans that deliver accurate ...
Clinical Data Managers
Salt Lake City, UT · On-site
$39K - $54K/yr
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Responsibilities Clinical Data Manager, II Develop data management plans that deliver accurate ...
Clinical Data Managers
Salt Lake City, UT · On-site
$39K - $54K/yr
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Responsibilities Clinical Data Manager, II Develop data management plans that deliver accurate ...
Clinical Data Managers
Campus, IL · On-site
$39K - $54K/yr
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Responsibilities Clinical Data Manager, II Develop data management plans that deliver accurate ...
Clinical Data Managers
Campus, IL · On-site
$39K - $54K/yr
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Responsibilities Clinical Data Manager, II Develop data management plans that deliver accurate ...
Clinical Data Managers
$39K - $54K/yr
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Responsibilities Clinical Data Manager, II Develop data management plans that deliver accurate ...
Clinical Data Managers
$39K - $54K/yr
Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Responsibilities Clinical Data Manager, II Develop data management plans that deliver accurate ...
Clinical Data Analyst
Princeton, NJ · On-site
He/she will ensure that processes and protocols are followed, regulations and company standards are followed, and the analysis goals are achieved, with quality and efficiency. A Clinical Data Analyst ...
Quick apply
Clinical Data Analyst
Princeton, NJ · On-site
He/she will ensure that processes and protocols are followed, regulations and company standards are followed, and the analysis goals are achieved, with quality and efficiency. A Clinical Data Analyst ...
Research Intern
Webster, TX · On-site
Description The Research Intern is an entry level clinical research position. The Intern will ... The Research Intern will also form other duties such as data entry, and administrative duties such ...
Research Intern
Webster, TX · On-site
Description The Research Intern is an entry level clinical research position. The Intern will ... The Research Intern will also form other duties such as data entry, and administrative duties such ...
Clinical Data Analyst
Princeton, NJ · On-site
He/she will ensure that processes and protocols are followed, regulations and company standards are followed, and the analysis goals are achieved, with quality and efficiency. A Clinical Data Analyst ...
Clinical Data Analyst
Princeton, NJ · On-site
He/she will ensure that processes and protocols are followed, regulations and company standards are followed, and the analysis goals are achieved, with quality and efficiency. A Clinical Data Analyst ...
Clinical Data Associate
Grand Rapids, MI · On-site
$70K - $85K/yr
Knowledge of current industry standards (e.g., GCP, ICH, CDISC/CDASH) * Proficiency with Microsoft ... Clinical Data Associate position. We value and appreciate our employees and will support you with ...
Clinical Data Associate
Grand Rapids, MI · On-site
$70K - $85K/yr
Knowledge of current industry standards (e.g., GCP, ICH, CDISC/CDASH) * Proficiency with Microsoft ... Clinical Data Associate position. We value and appreciate our employees and will support you with ...
Knowledge of current industry standards (e.g., GCP, ICH, CDISC/CDASH) * Proficiency with Microsoft ... Clinical Data Associate position. We value and appreciate our employees and will support you with ...
Quick apply
Knowledge of current industry standards (e.g., GCP, ICH, CDISC/CDASH) * Proficiency with Microsoft ... Clinical Data Associate position. We value and appreciate our employees and will support you with ...
Clinical Data Associate
Grand Rapids, MI · On-site
Knowledge of current industry standards (e.g., GCP, ICH, CDISC/CDASH) * Proficiency with Microsoft ... Clinical Data Associate position. We value and appreciate our employees and will support you with ...
Clinical Data Associate
Grand Rapids, MI · On-site
Knowledge of current industry standards (e.g., GCP, ICH, CDISC/CDASH) * Proficiency with Microsoft ... Clinical Data Associate position. We value and appreciate our employees and will support you with ...
Clinical Data Associate II
$75K - $90K/yr
Description The Clinical Data Associate will contribute to the performance of Clinical Data Management activities for assigned studies according to protocols, industry standards and guidelines, and ...
Clinical Data Associate II
$75K - $90K/yr
Description The Clinical Data Associate will contribute to the performance of Clinical Data Management activities for assigned studies according to protocols, industry standards and guidelines, and ...
Title: Clinical Data Manager Location: Irvine, CA Duration: 12 Months Job Functions and Duties ... Standard Operating Procedures (SOPs) and work practices. 8. Conduct their work activities in ...
Title: Clinical Data Manager Location: Irvine, CA Duration: 12 Months Job Functions and Duties ... Standard Operating Procedures (SOPs) and work practices. 8. Conduct their work activities in ...
Full-time
Medical, Retirement, PTO
Re-posted 2 days ago
Medpace rating
8.6
Based on 12 frontline employees who took The Breakroom Quiz
14th of 74 rated research
Job description
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Coordinator to join our Data Management team. This position involves working 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 knowledge and experience to further develop and grow your career even further, then this is the opportunity for you!
Data Coordinator Training and Development Program:The Medpace Data Management Training & Development (T&D) team will partner with each new hire to help develop those that are new to the industry and add continued support for those with experience. The program encourages team training while providing opportunities for one-on-one interactions directly with a T&D member. Each new hire will be provided with the following:
- Online training modules that include interactive exercises
- T&D led workshops that ensure understanding of Data Management processes and industry acronyms
- Opportunities to join other new professionals in the department within the training courses
- Direct support from one of the team's T&D members
- Validate entry database designs
- Report metrics and data trends on projects
- Identify data conflicts and issues on projects
- Work with personnel from global research sites to resolve data conflicts
- Reconcile data from multiple sources
- Create and update study documentation on projects
- Participate as part of a team on various projects
- Bachelor's degree in a Life Science or related field with strong attention to detail, excellent communication skills, ability to prioritize and multitask effectively and experience with Excel and Word.
- Previous experience working with research and statistical data is preferred ideally in a pharmaceutical or CRO setting.
TRAVEL: None
Medpace OverviewMedpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?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.
Purpose-Driven Work
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- Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
Collaborative Culture
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- Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
- Leadership throughout Medpace is both accessible and approachable
Continuous Growth & Development
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- Office based environment with on-site mentors
- Defined career paths with clear advancement opportunities
- Industry renowned onboarding and training programs designed to accelerate professional development
- Ongoing training and continuous learning opportunities throughout your career
- An environment that encourages employees to influence change, contribute ideas, and grow quickly
Other Employee Benefits
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- Competitive compensation programs that recognize and reward performance
- Comprehensive health, wellness, retirement, and PTO benefits
- Office based culture with occasional WFH that provides flexibility for eligible positions after training
- Company-sponsored social events and intramural sports
Cincinnati Headquarters Experience
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- A modern corporate campus designed to support collaboration and productivity
- Multiple on-site dining options in the heart of Madison Square
- Free on-site parking
- Convenient access to on-site 24-7 fitness and wellness facilities
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
Employment Type: OTHERAbout Medpace
Sourced by ZipRecruiter
Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.
Industry
Medical equipment and supplies manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Cincinnati, OH, US
Year founded
1992