Job as Sr Data Coord, CS Svcs in Quintiles

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.

Post: Sr Data Coord, CS Svcs

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:
Manage various data management projects and provide expertise as part of the Cardiac Safety Services data management team for efficient, quality data management products that meet customer requirements. Provide leadership to the team in the area of Data Management (DM).

RESPONSIBILITIES:

  1. Serve as a Data Team Lead and the main point of contact for various projects managed by the team.
  2. Ensure that all the deliverables are of expected quality standards and meet customer expectations.
  3. Attend study kick off meetings and internal/sponsor audits for assigned studies.
  4. Report on the quality of data collection and site issues to Data Management Team Leaders and apprise them of the status of each project.
  5. Interact with the Clinical Data Management personnel for project timelines, delivery of quality data and frequent project update teleconferences.
  6. Ensure that at the end of the study, all the Data Clarification forms are resolved, all data is “cleaned”, the data transfer is sent to the sponsor as per the agreed specifications, the data and the study files are completed and archived appropriately.
  7. Mentor other team members and ensure the completion of all required trainings.
  8. Assist in developing and implementing new technology / database revisions.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES -

  1. Thorough knowledge of the data management process and experience in specialized data management skills.
  2. Knowledge of operating procedures and work instructions and the ability to apply them in practice.
  3. Previous experience and proven competence in managing delivery of project through full data management study life-cycle.
  4. Knowledge of Computer application- MS Office, Oracle, SQL a plus.
  5. Good organizational, communication, and data management skills.
  6. Ability to establish and maintain effective working relationships with coworkers, managers and clients.

If you want to make an impact in the global research market, where we’re working to make a real difference in patient health, we ask you to apply now and join our team.

Qualifications:
MINIMUM REQUIRED EDUCATION AND EXPERIENCE -
Post Graduate degree in science or graduate in any discipline with 2-3 year experience in pharmaceutical company/ CRO industry; or equivalent combination of education, training and experience.
PHYSICAL REQUIREMENTS -
Extensive use of telephone and face-to-face communication requiring accurate perception of speech
Extensive use of keyboard requiring repetitive motion of fingers
Regular sitting for extended periods of time.

Additional Information:
Experience: 2-3 years
Education: B.Sc, M.Sc
Industry Type: Pharma/ Biotech/Clinical Research
Job Id: 1611448
Location: Karnataka-Bangalore

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