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Lead Clinical Research Specialist

2 months ago

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

We are looking for a dedicated Senior/Principal Clinical Research Associate to become an integral part of our Clinical Operations team. This role is essential for executing projects that contribute significantly to our organizational success. If you are seeking a fulfilling career where you can apply your skills and further your professional development, this position is tailored for you.

At Medpace, we foster a culture of expertise, empowering our teams to leverage their unique talents and experiences to take proactive approaches in research and problem-solving, ultimately supporting our business objectives. Our employees exemplify our values and commitment to client service, working diligently to meet high expectations and embrace challenges. In return, they enjoy engaging projects, opportunities for career progression, and recognition within our global framework. 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, verify the accuracy and completeness of reported trial data, and confirm compliance with approved protocols, GCP, and relevant regulatory requirements;
  • Conduct qualification, study initiation, routine monitoring, and study site close-out visits while ensuring site compliance with Medpace/Sponsor Standard Operating Procedures (SOPs);
  • Act as the primary contact for clinical investigators and site personnel;
  • Maintain strong collaboration and effective working relationships with internal cross-functional teams at Medpace;
  • Guarantee the quality completion of visit reports, follow-up correspondence, and the upkeep of study-related databases and ClinTrak Monitoring Portal.
Qualifications:
  • A Bachelor's degree in a health or science-related discipline, with a minimum of 5 years of clinical monitoring experience;
  • In-depth knowledge of practices and procedures related to all types of clinical monitoring visits, with practical application of this knowledge;
  • Proven ability to function as a Lead CRA when applicable, serving as a resource and mentor for new CRAs;
  • Ability to implement innovative ideas and solutions independently within their scope of 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 therapies through a scientific and disciplined approach. We utilize local regulatory and therapeutic expertise across various major areas, including oncology, cardiology, metabolic diseases, endocrinology, central nervous system, and anti-viral and anti-infective fields. With headquarters in Cincinnati, Ohio, we employ over 5,000 professionals across more than 40 countries.

Why Choose Medpace?

People. Purpose. Passion. Make a Difference Tomorrow.

The efforts we have made over the past 30+ years have positively influenced the lives of countless patients and families facing numerous diseases across all key therapeutic areas. The work we undertake today will enhance the lives of individuals living with illnesses and diseases 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 schedules;
  • 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 member of the Medpace team will review your qualifications and, if interested, will reach out with further details regarding the next steps.