Clinical Research Associate
Date posted: April 7, 2008
Location: Nationwide, NC
Job type: Full-time
Industry: Pharmaceutical
Description:
Clinsys Clinical Research, Inc.® is a full-service clinical research organization (CRO) that provides pharmaceutical, biotechnology and medical device companies with a broad range of clinical research services in support of Phase I-IV drug and device development. Due to our continued growth we are seeking CRAs to be based regionally from their home.
The successful candidate will monitor clinical trials in compliance with Clinsys’ and/or Sponsor’s Standard Operating Procedures (SOPs), as well as Code of Federal Regulations and ICH Good Clinical Practices. Assist in developing, managing and reporting on clinical trials and sites. Manage time, monthly calendars and deadlines, and adhere to expense and time policies & procedures.
Requirements for this position include Bachelors’ Degree (or equivalent), preferably in the life sciences, BS, RPh, or RN. Post-baccalaureate work or ACRP certification a plus, with 1 year of prior monitoring experience or 2-5 years of related clinical research experience.
Category: Pharmaceutical/Biotech
Company: Clinsys Clinical Research, Inc.
Clinsys Clinical Research, Inc.® is a full-service clinical research organization (CRO) that provides pharmaceutical, biotechnology and medical device companies with a broad range of clinical research services in support of Phase I-IV drug and device development, including project management, clinical monitoring, scientific and medical support, investigator and patient recruitment, site management, biostatistics, data management, drug safety, quality assurance, regulatory affairs, and medical writing.