Medpace is a globally renowned Clinical Research Organization (CRO) that provides end-to-end clinical trial services for the pharmaceutical, biotechnology, and medical device industries. Join us in our mission to accelerate the development of safe and effective medical therapeutics through our scientific expertise.
About Medpace
With over 30+ years of experience, Medpace has made significant contributions to the development of cutting-edge treatments across key therapeutic areas such as oncology, cardiology, infectious diseases, and more. Headquartered in Cincinnati, Ohio, Medpace operates in 40+ countries with a workforce of over 5,000 professionals. Our commitment to excellence ensures that we positively impact patients’ lives every day.
Job Responsibilities
As a Data Review Associate at Medpace, you’ll play a crucial role in clinical trial data management. Key responsibilities include:
- Conducting comprehensive manual reviews of clinical trial data.
- Developing clinical review guidelines tailored for specific therapeutic areas.
- Collaborating with the Data Management team to resolve data-related queries.
- Specializing in therapeutic areas such as:
- Oncology
- Hematology
- Infectious Diseases
- Endocrinology
- Metabolic Disorders
Qualifications
To qualify for the Data Review Associate role, you should meet the following criteria:
- A Bachelor’s Degree in Nursing or Medicine or an advanced clinical degree.
- Professional nursing experience, preferably in oncology and hematology.
- General understanding of clinical trial processes and experience with clinical data.
- Knowledge of using MedDRA and WHO Drug dictionaries is an advantage.
Required Skills
- Strong attention to detail for reviewing clinical data.
- Excellent collaboration and communication skills to interact with cross-functional teams.
- Ability to work effectively in a fast-paced environment.
- A strong grasp of therapeutic area guidelines and medical terminology.
