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Syneos Health Hiring for Central Monitor II | Remote

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Syneos Health

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences or Relevant Degree

IND-Remote

2+ Years

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Syneos Health is hiring for the role of Central Monitor II (RBQM / KRI review Exp) for an India remote position. This opportunity is suitable for candidates with relevant central monitoring experience who can work with RBQM-driven processes and support centralized monitoring activities for clinical studies.

Job Details

CompanySyneos Health
PositionCentral Monitor II
DepartmentAnalytical
LocationIND-Remote
Work ModeRemote
Employment TypeFull-time
Experience2+ Years

Job Description

Syneos Health is a fully integrated life sciences services organization focused on helping customers across drug development and commercialization. The Central Monitor II role is part of clinical solutions work involving centralized monitoring, RBQM processes, KRI review, data risk review, risk and issue management, and study data quality oversight.

The selected candidate will work with study teams and support the Central Monitoring Lead in the set-up and ongoing maintenance of the data analytical tool used for centralized monitoring.

Key Responsibilities

  • Work extensively in RBQM-driven processes.
  • Support the Central Monitoring Lead in the study-specific set-up and ongoing maintenance of the data analytical tool used for centralized monitoring.
  • Act as an RBM data analytical tool expert for conducting data risk review, risk and issue management.
  • Participate in the training of central and local study teams on RBQM and central monitoring processes.
  • Perform centralized monitoring of study data and maintain oversight of study, country, and site risk parameters according to the study monitoring plan.
  • Identify data quality trends indicative of systematic errors and potential study, country, or site performance issues.
  • Communicate trends, findings, implications, and recommended actions to relevant study team members within the data analytical tool.
  • Provide regular status reports to the study team.
  • Ensure proper documentation and archiving of instream data reviews, risk and issue management.
  • Share responsibility for data quality at the study, country, and site levels.

Experience

  • Minimum 2 years of relevant CM experience is required.
  • Experience in reviewing KRIs is preferred.
  • Cluepoints experience is preferable.
  • Candidate should be available for EMEA timing.

Additional Information

Syneos Health mentions career development and progression, supportive and engaged line management, technical and therapeutic area training, peer recognition, and a total rewards program as part of its people-focused work environment.

The company also states that its teams have worked over the past 5 years 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.

Company website:

http://www.syneoshealth.com

How to Apply

Interested candidates can apply online through the official Syneos Health Workday application link given below.

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