Clinical Data Reviewer II

Job Description

Primary Responsibilities Ensures the accuracy of client data by Conducting manual data review for data management customers at the direction of the Clinical Data Lead Issuing queries based on manual data review requirements for each assigned study using standard query wording under the guidance of more senior staff Participating in project team meetings as necessary Generating metrics and reports for current state of study database under the guidance of more senior staff Assisting in the management of the database cleaning and locking process Performing Clinical Data Management user acceptance testing as needed/ directed by the Clinical Data Manager Maintains quality service and departmental standards by Adhering to Clinical Data Management processes and standards by using implemented systems Reading , understanding and adhering to organizational Standard Operating Procedures (SOPs) Secondary Responsibilities Contributes to team effort by Working with internal staff to resolve issues Exploring new opportunities to add value to organization and departmental processes Helping others to achieve results Performing other duties as assigned Maintains Technical and Industry Knowledge by Attending and participating in applicable company - sponsored training Qualifications: Education: Diploma or equivalent , required , Associate s degree preferred Experience: 6 months experience in a data management role preferred , preferably in the pharmaceutical industry , or relevant experience in a related medical field , such as nursing Additional skill set: Strong problem - solving and organizational skills High attention to detail Demonstrated ability to manage multiple tasks simultaneously and complete work within allocated time frames. Excellent oral and written communication skills Other skills: The ability to contribute to a team environment with a high degree of professionalism and skill. Demonstrate flexibility within a dynamic , fast - paced , cross - functional team. Demonstrated ability to complete multiple tasks concurrently and deliver results in a fast - paced environment. Ability to perform under stringent timelines. Compliance : Awareness of organizational policies & procedures governing his/ her job responsibilities. Awareness and compliance of QMS & ISMS policies & procedures and their impact at his/ her job level. Should understand escalation matrix and escalate to the next level whenever incidents happen which are not in compliance with organizational , QMS & ISMS policies and procedures. Working Conditions: Normal office environment. Hours: Standard Hours 40 hours per week , one hour lunch , Monday Friday. Additional hours as needed. Willing to work in shifts as and when needed 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 Qualifications: Education: Bachelor s degree in Computer Science , Life Sciences or related field preferred , or equivalent experience required Experience: 2 years experience in comparable position within the pharmaceutical , biotech or CRO industry required Working knowledge of relational database organization and validation Familiarity with SAS desirable Experience working with office productivity tools including Word , Excel and Access preferred Understanding of clinical trial terminology desirable Proven ability in problem solving Additional skill set: Ability to work independently in a group setting; ability to adjust to changing priorities Excellent attention to detail Strong interpersonal and communication skills , both verbal and written Strong documentation and organizational skills Ability to project and maintain a professional and positive attitude Working conditions: Travel: 0 - 15% Lifting: 0 - 25lbs Other: Computer work for long periods of time 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 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.,

Keyskills :
sas cro qms roductivitytools writtencommunication lifesciences useracceptance standardoperatingprocedures musicmaking policiesprocedures clinicaldatamanagement useracceptancetesting communicationskills clinicaldata pharmaceuticalindustry ac