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Opportunity as Associate Medical Data Review Manager in Quintiles

 

Clinical courses

 

Clinical courses

Quintiles is the only fully integrated biopharmaceutical services company offering clinical, commercial, consulting and capital solutions worldwide. Our network of 23,000 engaged professionals in 60 countries around the globe works with an unwavering commitment to patients, safety and ethics — ensuring a higher level of healthcare for people. For our biopharmaceutical customers, we help them navigate risk and seize opportunities in an environment where change is constant.
Quintiles is consistently cited as the most favored contract research organization (CRO) in independent surveys of the bio pharma industry and was recently named “2009 CRO of the Year” by the prestigious SCRIP Awards.

Post:  Associate Medical Data Review Manager- 1616585

Job Description:
At Quintiles we help healthcare and biopharma companies improve their probability of success. We do this by connecting our scientific, therapeutic and analytics expertise with superior delivery. From advisory through operations, Quintiles and its affiliate companies is the world’s largest provider of product development and integrated healthcare services.

As one of FORTUNE’s ‘Most Admired Companies’ in 2016, we offer great opportunities for a career in world-leading clinical research. Our global projects, innovative tools and industry leading customers combined with outstanding support from our leadership team and clear career mapping allows you to make a difference in patient health.
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
1. Serve 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
2. Conduct in-stream data trend analysis in support of data quality and integrity (includes protocol compliance and targeted review of patient data)
3. Provide project management to the team in the area of Project Management and viewed as an expert in data management.
4. Drive the delivery of end-to-end study data quality and integrity.
5. 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.
6. Ensure data quality focus to audit readiness with Clinical Compliance and Systems Validation Compliance.
7. Define data capture requirements in line with protocol and reporting needs.
8. Maintain strong customer relationships
9. With guidance, track service performance and provide leadership to identify root causes of issues and implement remedial actions
10. Ensure timely follow-up and resolution of compliance issues
11. Serve as Subject Matter Expert (SME) 
12. Serve as POC/ Back-up POC 
13. Continuously look for opportunities to improve efficiency of tasks and quality of deliverables 
14.Provide therapeutic area/indication training for the project clinical team.  15.Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.

Required skills, knowledge & abilities

  • Good understanding of clinical/medical data. 
  • Knowledge of Medical Terminology, Pharmacology, Anatomy, and Physiology. 
  • 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, 
  • 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

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Qualifications   
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 5 years of relevant work experience; or equivalent combination of education, training and experience

PHYSICAL REQUIREMENTS 

  1. Extensive use of telephone and face-to-face communication requiring accurate perception of speech 
  2. Extensive use of keyboard requiring repetitive motion of fingers 
  3. Regular sitting for extended periods of time

Additional Information:
Experience: 5 years
Location: Karnataka-Bangalore
Education: B.Pharm, B.Sc, M.Pharm, M.Sc, MBBS
Industry Type: Pharma/ Biotech/Clinical Research
Last Date: 30th August, 2016

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