Job details
Job type full-time number of hires for this role 1
Qualifications
Bachelor`s (required)
Full job description
Worksites: south florida (must be willing to travel to worksites)
About us:
Cognitive research corporation (crc) is a privately held clinical research organization specializing in cns researchCrc was incorporated in 2006 and has grown to a team of 100We are a full-service cro providing comprehensive clinical operations, data management and statistical analysis servicesCrc brings to our clients, industry recognized expertise in cognitive assessment, driving assessment, evaluation of movement disorders, and application of neurological and psychiatric rating scalesWe have a truly exceptional biostatistics team and a robust network of clinical investigators who support phase 1 through phase 4 clinical trials.
Crc has contributed to the program design, drug development and registration of numerous fda and globally approved medicinesWe are committed to our employees and proactively support the professional growth of individualsWe are a diverse group of professionals that proactively foster a positive workplace culture to work, learn and contribute to bringing medicines to patients.
Position summary:
The clinical research associate is responsible for tracking and maintaining study specific non-crf databases and administrating clinical research projectsThis is accomplished by collecting documentation, site management, clinical contact, and reviewing crf’sThe cra is also responsible for maintaining relationships with investigators.
Key responsibilities:
Maintain a strong relationship with each investigator and clinical site staff.
Initiate, monitor, and close-out investigative sites in accordance with fda/ich regulations.
Track and maintain study specific non-case report form database
Administer clinical research projects; collect investigator documentation, site management, clinical contact, and prepare monthly status reports.
Review case report forms to identify erroneous, missing, or incomplete data.
Generate data queries to resolve problematic data to appropriate personnel, and review responses to assure the database is updated accordingly.
Report, write narratives, and follow-up on reported serious adverse events.
Verify study drug accountability; generate and track drug shipments and storage.
Travel as necessary, based on project needs.
Participate in the development of protocols and case report forms.
Perform data collection, retrieval, entry and clean up as necessary.
Negotiate study budgets with potential investigators.
Independently manage sites confirming clinical study site operations are completed under site procedures
Perform other duties as assigned by management.
Qualifications:
Bs/ba in appropriate field (e.gLife sciences, pharmacy, or nursing) or applicable education with relevant experience.
Experienced with numerous edc system
Experience in the pharmaceutical industry or hospital setting is preferable.
Ability to work and travel independently with minimal supervision.
Self-motivated attitude.
Computer competency (microsoft word and excel)
Good communication skillsGood command of written english.
Meticulous attention to details.
Job type: full-time
Benefits:
401(k)
Dental insurance
Health insurance
Paid time off
Vision insurance
Schedule:
Monday to friday
Application question(s):
Are you willing to travel 50-60%?
Education:
Bachelor`s (required)
Work location:
Multiple locations
Work remotely:
Yes
Work location: multiple locations
