Title: In-House Clinical Research Associate (CRA I)
Department: WorldCare Clinical
Reports To: Project Manager of Clinical Trial and Senior Project Manager
Status: Non-Exempt
Expectation for all Employees:
Support the organization’s mission, vision, and values by exhibiting the following behaviors: excellence and competence, collaboration, innovation, respect, commitment to our community, and accountability and ownership.
Job Summary:
Participate in monitoring and processing of clinical studies to ensure the day-to-day success of the Clinical Trials division. Follow instructions and pre-established guidelines to perform the functions of the job. The primary job functions do not typically require exercising independent judgment. May have direct contact with the sponsor and/or Contract Research Organization (CRO) and therefore must continuously represent WorldCare in a professional, courteous, time sensitive manner.
Essential Functions:
- Use Standard Operating Procedures (SOPs) concepts, practices and in a time sensitive manner the CRA will work to ensure the overall success of the designated Clinical Trial
- Consistently performs duties within established SOPs, Work Instructions (WI) and Study Specific Procedures (SSP)
- Work under direct supervision to ensure consistent performance
- Upon completion of training the employee must demonstrate the ability to work independently
- Report accurate information in a timely manner to incoming requests from sponsors and/or research organizations
- May recommend procedural or system changes to the Project Manager (PM) to improve the effectiveness of the trial’s operations
- Demonstrate consistent and cooperative service in support of the trial sponsor, staff, co-workers, and individuals outside of the organization
- Exhibit and maintain a team approach with a positive attitude
- Receive, track and process data from participating sites according to WI’s and SSP’s
- QC images in preparation of interpretation
- Digitize X-ray film from prior patient examinations
- Create Digital Files from MOD’s or other media types
- Insure the proper masking and blinding of patient demographics
- Assist the PM in training of new staff to SSPs and documentation used in the designated trial
- Recording clinical trial related information / data into the respective trial database
- Maintain and update trial tracking databases
- File, data entry, trial room set up, file storage, and any related activity to ensure the success of the Clinical Trials operations
- Must be able to lift 5 – 25 lbs
Qualification/Knowledge Requirements:
- Bachelors Degree in Sciences area preferred
- 0-1 years experience in the field or related area
- Computer skills and knowledge required
- Ability to organize and manage multiple priorities
- Strong customer orientation
- Excellent verbal/written communication skills, in the English language
To submit your cover letter and resume:
E-mail: careers@wcclinical.com
Fax: +1-513-352-9436
