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Reference #: R14571 Primary Responsibilities Interpreting radiology examinations according to standard medical practice, GCP guidelines, protocol and charter definition and according to standard Bioclinica SOPs Completing source documents accurately and promptly, according to the specific protocol requirements and following Bioclinica SOP Correcting entries on source documents and Case Report Forms (CRFs) in a timely manner as needed Participating in training sessions for the respective protocols Performing Image Quality Assessment Participating in Quality Assurance as needed Reviewing protocols, chartering and associated clinical and technical study documents as required Participating in InterReader and InterReader variability assessments when required Maintaining security of images, data and equipment. Participating in training and subsequently demonstrates competency in the operation of radiology research equipment Ensuring confidentiality of study protocols and subjects is maintained Participating in sponsor site visits and audits as requested Collaborating with management to resolve technical/radiological/study concerns and problems. Responsible for his/her continuing professional education Performing quality control on his/her work for completeness Identifying and participates in the performance improvement process Participating in the development, review and evaluation of SOPs and study specific procedures. Maintaining a safe work environment. Reporting workplace hazards immediately Other duties as assigned by the Chief Medical Officer

Secondary Responsibilities Maintains Quality Service and Departmental Standards by Reading, understanding and adhering to organizational Standard Operating Procedures (SOP) Establishing and enforcing departmental standards Reviewing and updating company SOPs related to Medical Affairs

Contributes to team effort by Exploring new opportunities to add value to organization and departmental processes Helping others to accomplish results

Qualifications: Education: Medical degree is required Advanced degree a plus Board Eligibility or Board Certification in Diagnostic Radiology and Nuclear Medicine or equivalent training demonstrating competency

Experience: 5+ years experience working with clinical trials and/or within pharmaceutical environment required Experience with multi-modality imaging projects required Experience with medical imaging software a plus Experience working with computer software including Word, Excel, Access and Project preferred

Additional skill set: Ability to work in group setting and independently; ability to adjust to changing priorities Strong motivational skills and abilities - promoting a team based approach Strong interpersonal and communication skills, both verbal and written Strong organizational skills and leadership skills Goal oriented Ability to project and maintain a professional and positive attitude

Working conditions: Travel: 10-20% Lifting: 0-15lbs Other: Computer work for long periods of time

This position description should not be deemed all inclusive. Additional requirements and expectations may be assigned. At all times, employees are expected to adhere to company policies and company SOPs.

EEO Statement Bioclinica is an equal opportunity employer. Bioclinica evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic

ERT is an equal opportunity employer and all qualified applicants receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.