**Work Schedule**
Other
**Environmental Conditions**
Office
We are vital links between an idea for a new medicine and the people who need it.
We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health.
You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients.
PPD's Centralized Monitoring group delivers a new approach to risk surveillance and centralized statistical monitoring, combining the power of statistical and analytical tools with expertise from operationally experienced staff to monitor and manage clinical study data.
Centralized Monitoring staff explores study data holistically to pinpoint meaningful signals, resulting in more efficient and effective issue resolution and a proactive approach to risk detection.
Using this data-driven approach, PPD can address study problems or site performance quickly, directing remediation activities where needed and positioning on-site monitoring activity in a targeted approach.
Centralized Monitoring evaluates data within and across studies, sites, countries and regions.
Our analytic approach provides insight into:
- Data errors, deviations
- Trends, outliers
- Unusual variation (or lack of variation)
- Potential data manipulation, fraud
- Other systematic errors or data integrity issues.
As a Senior Centralized Monitoring Analyst, you'll be supporting centralized statistical and risk surveillance activities on assigned trials.
At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team.
We offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees.
Summarized Purpose:
Identities and characterizes issues and trends in operational and patient clinical trial data using analytical or statistical tools.
Leverages operational experience and knowledge to evaluate issues and develop findings based on data analyzed to communicate issues and potential risks to project team members for follow-up action.
Begins to develop a Centralized Monitoring specialization and may execute Centralized Monitoring lead tasks or function as the lead on projects.
Essential Functions:
Independently reviews and analyzes clinical trial data using a variety of tools and systems in alignment with the centralized monitoring plan, flexing review assignments across the majority of different analyses.
Characterizes and tracks the evidence of issues, signals and potential risks.
Performs complex analyses and root cause analyses to connect related signal to risks, and responsible for ensuring delivery of high-quality, on time results.
May participate in lead activities, such as contribution to the development of the centralized monitoring plan, department risk assessment tool and cross-functional risk assessment meetings, risk reports and generating findings reports following review cycles.
May function as the Centralized Monitoring lead on some projects.
Provides training and guidance to junior team members.
Education and Experience:
Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years').
Prior experience in clinical monitoring, data management, biostatistics or related field in support of clinical trials is preferred.
In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered enough for an individual to meet the requirements of the role.
Knowledge, Skills and Abilities:
Strong attention to detail and skill with numbers
Strong analytical /problem-solving skills /judgment in decision making
Ability to work productively with direct supervision
Demonstrated ability to maintain a high degree of confidentiality with clinical data and client's proprietary data
Demonstrated flexibility and adaptability
Ability to work in a team environment and independently
Solid oral and written communication skills (English) with the ability to communicate effectively with a variety of internal and external customers, including project team, functional management and client contacts
Solid computer skills, with good knowledge of MS Office (Word, Excel, PowerPoint) and the ability to learn and use interactive computer systems
Comprehensive ability to extract pertinent information from standard study documentation, such as protocols, electronic study data systems and to identify trending of site/study data
Firm prioritization skills with ability to plan, monitor and manage workload fluidly in response to changing project demands
Strong understanding of project protocol, project documentation including Centralized Monitoring Plan and other functional plans
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