16 May

Operations Specialist Jobs Vacancy in Iqvia Bengaluru

Position
Operations Specialist
Company
Iqvia
Location
Bengaluru KA
Opening
16 May, 2018 30+ days ago

Iqvia Bengaluru urgently required following position for Operations Specialist. Please read this job advertisement carefully before apply. There are some qualifications, experience and skills requirement that the employers require. Does your career history fit these requirements? Ensure you understand the role you are applying for and that it is suited to your skills and qualifications.

Follow the online directions, complete all the necessary fields, and provide all relevant information so your application is submitted correctly. When you click the 'Apply this Job' button (open in new window) you will be taken to the online application form. Here you will be asked to provide personal and contact details, respond to employment-related questions, and show how you meet the key selection criteria.

Operations Specialist Jobs Vacancy in Iqvia Bengaluru Jobs Details:

Join us on our exciting journey!

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.
PURPOSE
Review, assess and process Lifecycle Safety data and information, across all service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members.

RESPONSIBILITIES
  • Receive, triage, review and process data from various sources on time, within budget and meet quality standards. Perform data entry for tracking and safety database, coding relevant medical terminology, writing descript narratives, generating queries pertinent to the case, performing quality control, assisting with reconciliation, driving case closure, coordinating translations and ensuring reports are sent to the customer within assigned deadlines. Pre-process material for endpoint committee or core laboratory adjudication. Preparation of material for submission of primary review.
  • Assess Lifecycle Safety data for report ability to relevant authorities, track reportable cases and report to regulatory authorities, ethics committees, institutional review boards, investigators, oversight groups per legislation, within timelines and in a format compatible to requirement. Liaise with local Quintiles offices to facilitate expedited reporting.
  • Receive and document incoming telephone calls, faxes or emails from investigative sites or other sources reporting Lifecycle Safety data.
  • Process Lifecycle Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements.
  • Assist operations team with tasks, provide for back-up to the operations team, assist in generation of status reports, providing project metrics, drafting project instructions/guidelines and assist in implementation of new processes.
  • Contribute under guidance of senior staff to individual deliverables in the field of Safety Publishing, Risk Management, Safety Surveillance and Medical Information, or other service lines as appropriate.
  • Liaise with different functional team members, e.g. project management, clinical, data management; health care professionals e.g. investigators, medical monitors, site coordinators and designees to address project related issues.
  • Attend project team meetings and provide feedback to operations manager on any challenges/issues or successes.
  • May liaise with client in relation to details on day to day process of cases.
  • Perform operational and collaborative LSM task as directed by Lifecycle Safety Infrastructure.
  • Ensure compliance to Quintiles high quality standards and work with LSM constructively in a matrix framework to achieve project and customer deliverables.
  • Executes administrative operational tasks as required e.g. committee and laboratory management.
  • Collaborate with SO and LSM to help achieve operational departmental goals i.e. understands metrics appropriate to quality document management and assist in the achievement of productivity utilization and realization metrics.
  • Read and acknowledge all necessary Quintiles standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion and documented. Work towards ensuring your individual training plan and training transcript are reconcilable.
  • Perform other duties as assigned.

    REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
  • Working knowledge of Lifecycle Safety services. Familiarity with functionality of the Quintiles Regulatory Database and Endpoint Tracking Database.
  • Basic knowledge of applicable global, regional, local clinical research regulatory requirements; i.e. Good Clinical Practice (GCP) and International Conference of Harmonization (ICH) guidelines, SOPs.
  • Ability to meet strict deadlines; manage competing priorities and changing demands.
  • Sound organization and time management skills.

  • Ability to follow instructions/guidelines, work independently and on own initiative.
  • Good attention to detail and accuracy and maintain high quality standards.
  • Demonstrate good IT skills.
  • Effective written and verbal communication skills.
  • Ability to be flexible and receptive to changing process demands.
  • Willingness and aptitude to learn new skills across Lifecycle Safety service lines.
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients.

Job Requirements

MINIMUM REQUIRED EDUCATION AND EXPERIENCE
High School Diploma with 5 years’ relevant experience or Bachelor’s Degree in scientific or healthcare discipline or equivalent combination of education, training and experience.

PHYSICAL REQUIREMENTS
  • Extensive use of keyboard requiring repetitive motion of fingers.
  • Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
  • Regular sitting for extended periods of time.
  • May require occasional travel.
We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.

Whatever your career goals, we are here to ensure you get there!


We invite you to join IQVIA™.


Job ID: 1807380


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