Regional CRA II
Job Code: CSA1115A
Nationwide – 1-1½ years of solid monitoring
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 and/or medical devices. Represents company in the
global medical research community and develops collaborative relationships
with investigative sites and client company personnel. Required to travel
60-70% on average.
Education and Experience
- Bachelor’s Degree in life sciences or related field or certification
in a related allied health profession from an appropriately accredited
institution (i.e.: RN, MT, PA, RPh, RT)
- Minimum one year as a clinical monitor.
- In some cases, a combination of education and prior directly related
experience may be considered as equivalent to the above requirements
provided that the individual possesses the following knowledge, skills,
and abilities to perform the job requirements satisfactorily.
Knowledge, Skills and Abilities
- Previous successful completion of or ability to successfully
complete company training program
- Effective clinical monitoring skills
- Demonstrated ability to attain and maintain a working knowledge of
GCPs and applicable SOPs
- Basic computer skills and ability to learn and become proficient
with appropriate software
- Demonstrated understanding of medical terminology
- Effective oral and written communication skills with ability to
communicate effectively with medical personnel
- Strong customer focus and excellent interpersonal skills
- Strong attention to detail
- Proven flexibility and adaptability
- Ability to work in a team environment and independently as needed
- Valid Driver’s License and ability to qualify for and maintain a
corporate credit card with sufficient credit line to allow for extensive
business travel
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