Sr Data Ops Technical Specialist

Syneos Health, Inc.

Hyderabad

Vor Ort

INR 1.800.000 - 2.400.000

Vollzeit

Vor 9 Tagen

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Zusammenfassung

Syneos Health is seeking a Sr Data Ops Technical Specialist in Hyderabad to lead data management activities and ensure global best practices across systems and databases. The role emphasizes hands-on PDM leadership, collaboration with internal teams, and compliance with study timelines.

You will participate in audits, sponsor meetings, and develop data collection guidelines, while mentoring junior staff. The position requires 7+ years in data management and willingness to travel up to 25%.

Aufgaben

  • 7+ years of Data Management experience, with at least 2 years of hands-on experience leading PDM activities/projects.
  • Support DM to ensure processes in relation to systems/databases are consistent and that best practices are maintained globally.
  • Assist with developing, monitoring and enforcing productivity, quality standards and efficiencies, input into the development of project and timeline metrics.
  • Maintain awareness of potential out of scope work for assigned projects and support Lead Clinical Data Manager (LCDM) as appropriate.
  • Participate in and present at internal, sponsor, third-party, and investigator meetings.
  • Participate in and support internal and external audits and inspections.
  • Support the development of User Test Plans for data entry screens, electronic edit checks, data listings, import/export programs and medical coding.
  • Support the release of tested clinical data databases and updates to the production environment.
  • Support the development of CRF and eCRF completion guidelines.
  • Support the development and review of specifications for listings and summaries (other than for statistical reporting requirements) from CRF databases and external sources.
  • Participate in the development of departmental technologies, SOPs, processes and procedures.
  • Support and participate in the testing and integration of new technologies within Data Operations.
  • Maintain documentation on an ongoing basis and ensure that all TMF filing is correct and up to date.
  • Train and mentor Data Management staff.
  • Maintain proficiency in Data Management systems and processes through regular training.
  • May represent Data Operations in company-wide initiatives
  • Performs other work-related duties as assigned. Minimal travel may be required (up to 25%)

Jobbeschreibung

Sr Data Ops Technical Specialist

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.

Discover what your 25,000 future colleagues already know:

Why Syneos Health
  • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
  • We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
  • We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.
Job Responsibilities
  • Required: 7+ years of Data Management experience, with at least 2 years of hands-on experience leading PDM activities/projects.
  • Supports DM to ensure processes in relation to systems/databases are consistent and that best
  • practices are maintained globally. Can consult with internal functional teams and sponsors as a SME
  • Assists with developing, monitoring and enforcing productivity, quality standards and efficiencies, input into the development of project and timeline metrics
  • Maintains awareness of potential out of scope work for assigned projects and supports Lead Clinical Data Manager (LCDM) as appropriate
  • Participates in and presents at internal, sponsor, third-party, and investigator meetings
  • Participates in and supports internal and external audits and inspections
  • Supports the development of User Test Plans for data entry screens, electronic edit checks, data listings, import/export programs and medical coding
  • Supports the release of tested clinical data databases and updates to the production environment
  • Supports the development of CRF and eCRF completion guidelines
  • Supports the development and review of specifications for listings and summaries (other than for statistical reporting requirements) from CRF databases and external sources
  • Participates in the development of departmental technologies, SOPs, processes and procedures
  • Supports and participates in the testing and integration of new technologies within Data Operations
  • Maintains documentation on an ongoing basis and ensures that all TMF filing is correct and up to date
  • Train and mentor Data Management staff
  • Maintains proficiency in Data Management systems and processes through regular training.
  • May represent Data Operations in company-wide initiatives
  • Performs other work-related duties as assigned. Minimal travel may be required (up to 25%)
Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

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