Medpace Remote Work Values

Daily Duties at Medpace Remote:

Coordinate and oversee clinical trial submissions activities and maintain submission timelines globally Maintain ongoing Sponsor contact for submission-specific issues Independently interact with Sponsor, sites, IRB/ECs, regulatory agencies and Medpace team Provide submission advice and guidance to Medpace team to ensure compliance with appropriate regulations and requirements Prepare project/country-specific Informed Consent templates and negotiate/review content changes from sites Provide oversight of Clinical Trial Submissions Coordinators and Project Assistants Review pertinent regulations and guidances to develop proactive solutions to regulatory issues and challenges

What they like about Medpace Remote:

You highly value a work environment built on a formal structure, rules, and regulations. You do not enjoy the unpredictability of shifting priorities and deadlines that upset your routine. You require and enjoy direction, input and accountability as part of your work environment. You have a strong need to participate in making key decisions and feel left out if your superiors or co-workers do not seek your input when making decisions. You thrive on providing good customer service to both internal or external customers, and doing so makes you feel good.

Tags

Clinical Research, Business Management, Clinical Trials, Study Start Up, Sponsor Collaboration, Site Activation, Regulatory IRB/ EC, CLinTrak, goBalto, CTMS, Regulatory Submissions Manager

Skills

Lean Six Sigma Yellow Belt, Line Manager 10 years, Global Regulatory Submissions, Sponsor/ Client Facing, Drive Study Start Up Timelines, Problem solve to fast site activation, Postive Team Leader, Participate with Bid Defense , Kick Off, Investigator and Face 2 Face Meetings, Risk escalation and mitigations

These are some of the questions we asked our climbers about their experiences with Medpace Remote: