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Lead Clinical Research Specialist

2 months ago

Bristol, Maine, United States Medpace Full time
Position Overview:

We are actively looking for a full-time, Senior Clinical Research Associate to enhance our Clinical Operations team. This position plays a crucial role in executing tasks and projects that are essential to the organization's success. If you are seeking a fulfilling career where you can leverage your expertise and further develop your professional skills, this opportunity is tailored for you.

At Medpace, we foster a culture of expertise, empowering our teams to utilize their unique talents and experiences to adopt a proactive approach to research, problem-solving, and ultimately supporting our business partners. Our employees exemplify our values and our commitment to serving our clients. They are dedicated, understand our high standards, and rise to the occasion. In return, they are rewarded with engaging projects, opportunities for career advancement, and recognition within our global network. These are just a few reasons why skilled professionals choose to be part of the Medpace family.

Key Responsibilities:
  • Ensure the protection of subjects' rights and well-being, confirm that the reported trial data is accurate, complete, and verifiable from source documents, and guarantee that the trial is conducted in accordance with the approved protocol, GCP, and applicable regulatory requirements;
  • Oversee site compliance while performing qualification, study initiation, routine monitoring, and study site close-out visits in alignment with Medpace/Sponsor Standard Operating Procedures (SOPs);
  • Act as the primary point of contact for clinical investigators and site personnel;
  • Maintain close collaboration and effective working relationships with internal cross-functional teams at Medpace;
  • Ensure the quality completion of visit reports, follow-up correspondence, and upkeep of study-related databases and ClinTrak Monitoring Portal.
Qualifications:
  • Bachelor's degree in a health or science-related field with a minimum of 5 years of experience in clinical monitoring;
  • Thorough understanding of practices and procedures related to all types of clinical monitoring visits, including practical application of this knowledge;
  • Proven ability to function as a Lead CRA (as applicable) and serve as a resource for new CRAs, facilitating training and mentorship;
  • Proactively implement new ideas and solutions within their authority.
About Medpace:

Medpace is a comprehensive clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device sectors. Our mission is to expedite the global development of safe and effective medical therapeutics through a scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across various fields, including oncology, cardiology, metabolic diseases, endocrinology, central nervous system, and anti-viral and anti-infective areas. Headquartered in Cincinnati, Ohio, we employ over 5,000 individuals across more than 40 countries.

Why Choose Medpace?

People. Purpose. Passion. Make a Difference Tomorrow.

The work we have accomplished over the past 30 years has positively influenced the lives of countless patients and families facing numerous diseases across all key therapeutic areas. The efforts we undertake today will enhance the lives of individuals living with illness and disease in the future.

Medpace Benefits:
  • Hybrid work-from-home options (dependent upon position and level);
  • Competitive PTO packages;
  • Company-sponsored employee appreciation events;
  • Employee health and wellness initiatives;
  • Flexible work schedule;
  • Competitive compensation and benefits package;
  • Structured career paths with opportunities for professional growth.
Awards:
  • Recognized by Forbes as one of America's Most Successful Midsize Companies in recent years;
  • Consistently honored with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.
Next Steps:

A Medpace team member will review your qualifications and, if there is mutual interest, you will be contacted with further details regarding the next steps.