Sr. Clinical Data Reviewer
Ver: 106
Dia de atualização: 06-05-2024
Localização: Itanagar Arunachal Pradesh Dibrugarh Assam
Categoria: R & D IT - Software
Indústria: Information Technology Services Hospital & Health Care Pharmaceuticals
Posição: Entry level
Tipo de empregos: Full-time
Conteúdo do emprego
Primary ResponsibilitiesEnsures the accuracy of client data by
- Conducting manual data review for Clinical Data Management customers at the direction of the Clinical Data Lead
- Independently issuing queries based on manual data review requirements for each assigned study
- Participating in project team meetings as necessary
- Generating metrics and reports for current state of study database
- 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
- Performing external data reconciliation at the direction of the Clinical Data Lead
- Performing Clinical Data Management quality review procedures
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:
- Diploma or equivalent, required, Associate’s degree preferred
- 1+ year experience in a data management role preferred, preferably in the pharmaceutical industry, or relevant experience in a related medical field, such as nursing
- 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
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
Collaboration, Continuous Learning, Critical Thinking, Organizational Awareness, Results Orientation, Service Orientation
Data limite: 20-06-2024
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