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Medical Data Review Manager _ Part-Time

IQVIA Holdings Inc.

Rockville, Maryland

IQVIA is changing an entire industry through inspired innovation. Our People make the difference. We believe that great ideas can come from anywhere. Great products come from great ideas. And great ideas come from great people. We look for the very best people and then give them meaningful work to do. Join IQVIA and help us make the world a better place.

PURPOSE

Provide expert skills as part of a Medical Data Review team to provide efficient, quality Medical Data Review products that meet customer needs.

RESPONSIBILITIES

 Serves as a Subject level Data reviewer (SLDR) and Identify any anomalies in patient reported data by performing Subject Level Data Review that require further investigation with the clinical site to determine overall accuracy

 Conducts in-stream data trend analysis in support of data quality and integrity (includes protocol compliance and targeted review of patient data).

 Ensures data quality focus to audit readiness with Clinical Compliance and Systems Validation Compliance.

 Defines data capture requirements in line with protocol and reporting needs.

 Provide project management to the team in the area of Project Management and viewed as an expert in data management.

 Drive the delivery of end-to-end study data quality and integrity

 May act as a clinical data scientist for performing data analytics by reviewing the visualizations, identify potential issues of concern and present at multi-disciplinary team meetings and external meetings

 Provide medical, clinical, and scientific advisory expertise.

 Maintain strong customer relationships.

 With guidance, track service performance and provide leadership to identify root causes of issues and implement remedial actions.

 Ensure timely follow-up and resolution of compliance issues.

 Serve as Subject Matter Expert (SME).

 Serve as POC/ Back-up POC.

 Continuously looks for opportunities to improve efficiency of tasks and quality of deliverables.

 Provide therapeutic area/indication training for the project clinical team.

 Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

 Good understanding of clinical/medical data.

 Proven expertise in the proactive identification of issues.

 Demonstrated ability to plan, organize and manage resources to bring to successful completion specific study or project goals and objectives in accordance with defined quality and time based metrics.

 Proven ability to work within a matrix team environment requiring minimum level of supervision

 Attention to detail

 Interpersonal and analytical skills

 Knowledge of Medical Terminology, Pharmacology, Anatomy, and Physiology.

 Must have Medical but also an operational focus towards metrics and status information to take the appropriate actions to resolve.

 Excellent communication, interpersonal, customer service, and teamwork skills.

 Excellent organizational and problem-solving skills.

 Excellent project management skills and coaching skills.

 Ability to work with minimal supervision, using available resources.

 Ability to work on multiple projects and manage competing priorities.

 Strong customer focus skills.

 Ability to establish and maintain effective working relationships with coworkers, managers and clients.

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

Medic with 5 year college degree or MBBS; or Bachelor’s degree in clinical, biological, mathematical sciences, or related field, or nursing qualification, with 7 years of relevant work experience; or equivalent combination of education, training and experience. Experience in clinical data sciences at a CRO, pharmaceutical company or other medical environment with demonstrated leadership.


At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.

IQVIA, Inc. provides reasonable accommodations for applicants with disabilities.  Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIA’s Talent Acquisition team at workday_recruiting@iqvia.com to arrange for such an accommodation.

Job posted: 2021-04-28

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