Spotlight Employers
Clinical Site Managers
The Clinical Site Manager has a variety of broad responsibilities. First and foremost, the Clinical Site Manager is responsible for the day-to-day operations at a clinical trial site as well as the recruitment, supervision and management of all the clinical staff. The Clinical Site Manager is also the individual ultimately responsible for patient enrollment at a clinical trial site. Most likely reporting to the Chief Operations Officer (COO), the Clinical Site Manager must also ensure that all clinical trial processes adhere to Good Clinical Practices as well as other imposed regulations and guidelines. This high-profile role is also charged with closely monitoring all clinical research and reporting to the COO and other stakeholders as to the ongoing progress and findings.
Because this line of work is so reliant upon sharp business acumen, management experience is almost always required in addition to extensive experience in the clinical environment. A four-year degree or higher is also required.
Employment Outlook
Career opportunities for Clinical Site Managers are found in hospitals, physicians’ offices, contract research organizations, biomedical research organizations and institutions, sectors of the government, and specialty disease centers and pharmaceutical and medical device suppliers. With the rapid growth of the healthcare industry, Clinical Research Manager positions are expected to increase 14% or more in the next 10 years.
Current Job Openings
Drug Safety Associate
- Assist with the overall Clinical Safety and/or Pharmacovigilance operations associated with products including the entire adverse events process: which may include...(more)
Clinical Research Coordinator (CRC)
General Summary of Duties
Provides professional nursing care and monitoring for research patients. Performs duties involved in...(more)
Clinical Research Associate (CRA)
Title: Clinical Research Associate
Country United States
Description
- Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 - 50% travel) for GCP...(more)
Clinical Project Manager
Responsibilities
The qualified candidate will be an experienced Clinical Project Manager that is capable of handling...(more)
Clinical Research Coordinator (CRC)
Job Summary-
The Research Nurse Coordinator manages clinical research projects for Principal Investigator via study protocol within the University, competently performs the nursing...(more)
Biostatistician
:
BIOSTATISTICAL ANALYST
Under general supervision the Biostatistical Analyst analyzes and interprets confidential data from a variety of sources. The Analyst is capable of...(more)
Clinical Data Analyst
Description
Ingenix delivers Intelligence for Health Care. A UnitedHealth Group company, Ingenix unites the brightest...(more)
Clinical Research Associate (CRA)
Exciting regional home-based permanent opportunity with one of the fastest growing International Clinical Research Organizations in the country. CRA's with 2-3 year of oncology monitoring...(more)
Clinical Research Associate (CRA)
The Clinical Research Associate II performs and coordinates all aspects of the clinical monitoring process in accordance with GCPs and global SOPs to assess the safety and efficacy of...(more)
Clinical Data Manager
Minimum Qualifications :
- Five years of experience OR the equivalent combination of education and experience with a...(more)