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
Clinical Research Associate (CRA)
This position performs and coordinates all aspects of the clinical monitoring process in accordance with GCPs and global SOPs to assess the safety and efficacy of investigational products...(more)
Biostatistician
The Biostatistician Acts as lead statistician on projects of moderate to large size and complexity; support lead statistician on very large, complex studies. May have staff management and/or...(more)
Clinical Research Associate (CRA)
This position performs and coordinates all aspects of the clinical monitoring process in accordance with GCPs and global SOPs to assess the safety and efficacy of investigational products...(more)
Biostatistician
SENIOR BIOSTATISTICIAN
North Wales, PA
Exempt Position
...(more)
Biostatistician
Job Summary
Act as the lead or back-up statistician for Kendle projects with low to moderate complexity. May act as the supportive statistician for Kendle projects with...(more)
Clinical Data Coder
Job Summary
Serves as a resource primarily for the local Kendle Clinical Data Management (CDM) organization regarding the coding of clinical trials data (i.e. adverse...(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)
Clinical Research Associate
Description:
Assists in the design, planning, and implementation of clinical research projects. Coordinates activities between company, Contract...(more)
Clinical Data Manager
:
Under general supervision, the Clinical Data Manager reviews data; assists in database design and testing; designs CRFs and guidelines; designs and tests logic checks;...(more)
Clinical Data Manager
Job Summary
Serves as the primary Kendle CDM contact with Sponsors and represents CDM on project teams. Responsible for project timelines, deliverables, financial...(more)