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Virtual CRC Event - May 1, 2024 Job in Cincinnati, Ohio US
Monster
 
 
 
 

Job Summary

Company
Medpace, Inc.
Location
Cincinnati, OH
Industries
Government and Military
Job Type
Full Time
Employee
Years of Experience
Less than 1 Year
Job Reference Code
78946291

Virtual CRC Event - May 1, 2024

About the Job

Virtual CRC Event - May 1, 2024


Job Locations

United States | United States-TX-Irving (Dallas) | United States-NY-New York | United States-NC-Raleigh | United States-MI-Detroit | United States-Los Angeles | United States-CA | United States-MA-Boston | United States-WA-Seattle | United States-UT-Salt Lake City | United States-MO | ...




Category

Medpace Recruitment Events


Job Summary




Medpace will be hosting a Virtual Networking Event to highlight our exciting Clinical Research Associate opportunites! We are seeking qualified Clinical Research Coordinators and Research Nurses to attend.

When: Wednesday, May 1, 2024 from 6-7 pm ET on Microsoft Teams.

**More details regarding the format of this virtual event will be provided should you be selected to attend.

Clinical Research Coordinators/Research Nurses wanted at Medpace! Become a CRA and join our growing team!

This is an exciting opportunity for clinical research professionals with at least 1.5 years of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings at Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a competitive salary.



WE OFFER THE FOLLOWING

Competitive travel bonus;
Equity/Stock Option program;
Training completion and retention bonus
Annual merit increases;
401K matching;
The opportunity to work from home;
Flexible work hours across days within a week;
Retain airline reward miles and hotel reward points;
Home office furniture allowance, laptop, mobile phone with hotspot for internet access anywhere;
In-house travel agents and reimbursement for airline club;
Opportunity for leadership positions - Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager, and many more;
CRA training program (PACE);
Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts;
In-house administrative support for all levels of CRAs; and
Opportunities to work with international team of CRAs.


Responsibilities




Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;
Communication with the medical site staff including coordinators, clinical research physicians, and their site staff;
Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements;
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;
Verification that the investigator is enrolling only eligible subjects;

Regulatory document review;
Medical device and/or investigational product/drug accountability and inventory;
Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
Assess the clinical research site's patient recruitment and retention success and offering suggestions for improvement; and
Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.


Qualifications




Must have a minimum of a Bachelor's degree in a health or science related field;

Experience as a Clinical Research Coordinator (minimum 1.5 years);

Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely;
Must maintain a valid driver's license and the ability to drive to monitoring sites;
Proficient knowledge of Microsoft Office;
Strong communication and presentation skills; and
Must be detail-oriented and efficient in time management.


Medpace Overview




Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.


Why Medpace?




People. Purpose. Passion. Make a Difference Tomorrow. Join Today

The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

Hybrid work-from-home options (dependent upon position and level)
Competitive PTO packages - starting at 20+ days
Company-sponsored employee appreciation events
Employee health and wellness initiatives
Wellness rooms and huddle rooms
Flexible work schedule
Competitive compensation and benefits package
Structured career paths with opportunities for professional growth
Discounts for local businesses

Awards:

Recognized by Forbes as one of America's Best Mid-size Companies in 2021, 2022, and 2023
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility



What to Expect Next:

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

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