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Centralized Monitoring Analyst (I, II)

Job Qualification:

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 2+ 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 sufficient for an individual to meet the requirements of the role

Knowledge, Skills and Abilities:

Capable of applying fundamental knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, global SOPs and client expectations

Strong attention to detail and skill with numbers

Solid analytical /problem-solving skills /judgment in decision making

Ability to work productively with direct supervision

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

Good oral and written communication skills (English) with the ability to communicate with a variety of internal customers, including project team

Good computer skills, with knowledge of MS Office (Word, Excel, PowerPoint) and the ability to learn and use interactive computer systems

Ability to extract pertinent information from standard study documentation, such as protocols, electronic study data systems with the ability to learn to identify trending of site/study data

Good Prioritization skills with ability to plan, monitor and manage workload fluidly in response to changing project demands

Good understanding of project protocol, project documentation including Centralized Monitoring Plan and other functional plans

Demonstrated proficiency in expanding analysis, knowledge and quality in findings

Good working knowledge of the roles, functions and process of conducting clinical trials

Good understanding of medical/therapeutic area knowledge and of medical terminology

Working Environment:

PPD values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:

Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.

Able to work upright and stationary and/or standing for typical working hours.

Able to lift and move objects up to 25 pounds

Able to work in non-traditional work environments.

Able to use and learn standard office equipment and technology with proficiency.

May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.

Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

PPD Defining Principles:

- We have a strong will to win - We earn our customer's trust - We are gamechangers - We do the right thing - We are one PPD

If you resonate with our five principles above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world's most urgent health needs, then please submit your application - we'd love to hear from you.





Diversity Statement

PPD is proud to be an affirmative action employer that values diversity as a strength and fosters an environment of mutual respect. PPD is committed to providing equal employment opportunities without regard to age, race, color, pregnancy, national origin, religion, sex, gender identity, sexual orientation, disability, veteran status or status within any other protected group.

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