Project Coordinator, Data Monitoring - Entry Level

Medpace, Inc.; Cincinnati (OH); In loco; USD 38.000 - 48.000; Tempo pieno

Vantaggi offerti da questo lavoro

Competitive compensation programs

Comprehensive health, wellness, and 18

PTO benefits

Office-based culture with occasional W

Descrizione del lavoro

Medpace, a full-service clinical CRO headquartered in Cincinnati, invites applications for an Entry Level Project Coordinator to join the Internal Data Monitoring team for data-related support in ongoing trials. This office-based role emphasizes confidentiality, organization, and collaboration with physicians and industry experts.

The position offers on-site work with training and opportunities for growth within clinical development.

Competenze

• Bachelor's degree in life science or health related field.
• Excellent written and verbal communication skills.
• Proficient knowledge of Microsoft Word, Excel, and PowerPoint.
• Exposure to/knowledge of medical terminology and healthcare systems.

Mansioni

• Provide administrative, logistical, and coordinating support for Data Monitoring Committees (DMCs), including scheduling meetings, distributing unblinded data, and documenting decisions and outcomes.
• Partner with the Internal Medpace team to identify and contract independent physicians and industry experts to assemble DMCs to review safety and efficacy data for ongoing trials.
• Assist in the development and maintenance of study specific documents describing DMC processes and procedures.
• Maintain the study blind and handle unblinded materials with discretion to ensure confidentiality.
• May be responsible for other projects and responsibilities as assigned.

Conoscenze

Communication skills

MS Office Suite

Medical terminology

Formazione

Bachelor's degree in life science or health related field

Strumenti

Microsoft Office Suite

Descrizione del lavoro

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Entry Level Project Coordinator to join our Internal Data Monitoring 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

• Provide administrative, logistical, and coordinating support for Data Monitoring Committees (DMCs), including scheduling meetings, distributing unblinded data, and documenting decisions and outcomes
• Partner with the Internal Medpace team to identify and contract independent physicians and industry experts to assemble DMCs to review of safety and efficacy data for ongoing trials
• Assist in the development and maintenance of study specific documents describing DMC processes and procedures
• Maintain the study blind and handle unblinded materials with discretion to ensure confidentiality
• May be responsible for other projects and responsibilities as assigned

Qualifications

• Bachelor's degree in life science or health related field;
• Excellent written and verbal communication skills;
• Proficient knowledge of Microsoft Word, Excel, and PowerPoint; and
• Exposure to/knowledge of medical terminology and healthcare systems

Medpace Overview

Medpace 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

• Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

• 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

• 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

• 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

• 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.