We are seekingAdvanced Nurse Practitioners/ Clinical Nurse Specialists with Haematology/Oncology experience who are interested in being at the forefront of new treatments for patients with haematologic and oncologic diseases. This role will work side by side with our physicians, serving as clinical expert, to support our project teams in clinical research studies (no direct patient care). Experience in the medical management of patients with these diseases, including prescriptive authority, is preferred. Experience in clinical research is preferred.
Responsibilities
* Develop and implement disease-specific and clinical education for internal teams
* Review study and study participant clinical safety data (e.g. laboratory, medications, medical history) as an integral part of the study's medical monitoring team
* Review assigned protocols for scientific and participant safety matters and risks
* Attend pre-study and study-related meetings with project teams, providing clinical expertise
* Assist the Clinical Operations team with activities related to study participant recruitment, screening and study conduct
* Participate in new business activities by providing clinical input in Medpace's written proposals for conducting a client's clinical trial
* Serve as a clinical expert in business presentations to new clients
Qualifications
* Masters or doctorate degree in nursing; or equivalent qualifications;
* Nursing and Midwifery Council registration and NMC pin number;
* Significant experience as an advanced nurse practitioner/clinical nurse specialist within haematology/oncology/haem-oncology;
* Proficient knowledge of Microsoft Office products including Outlook, Word, and Excel;
* Clinical research experience preferred; and
* Evidence of autonomous clinical or research work at senior level.
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 Us 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
* Flexible work environment
* Competitive compensation and benefits package
* Competitive PTO packages
* Structured career paths with opportunities for professional growth
* Company-sponsored employee appreciation events
* Employee health and wellness initiatives
Awards
* Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
* 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.
* Masters or doctorate degree in nursing; or equivalent qualifications;
* Nursing and Midwifery Council registration and NMC pin number;
* Significant experience as an advanced nurse practitioner/clinical nurse specialist within haematology/oncology/haem-oncology;
* Proficient knowledge of Microsoft Office products including Outlook, Word, and Excel;
* Clinical research experience preferred; and
* Evidence of autonomous clinical or research work at senior level.
* Develop and implement disease-specific and clinical education for internal teams
* Review study and study participant clinical safety data (e.g. laboratory, medications, medical history) as an integral part of the study's medical monitoring team
* Review assigned protocols for scientific and participant safety matters and risks
* Attend pre-study and study-related meetings with project teams, providing clinical expertise
* Assist the Clinical Operations team with activities related to study participant recruitment, screening and study conduct
* Participate in new business activities by providing clinical input in Medpace's written proposals for conducting a client's clinical trial
* Serve as a clinical expert in business presentations to new clients
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