RSM (Level I)
PPD is a leading global contract research organization. At PPD we are passionate, deliberate, and driven by our purpose – to improve health.
Remote Site Monitoring and Management (RSMM) blends on and off-site monitoring functions, providing efficiency to our clients. The RSMM group provides global time zone coverage and optimizes technology. Working in the RSMM group, you will contribute directly to PPD’s strategy to bend the time and cost curve of drug development by providing adaptive and intelligent monitoring services to our clients.
As a Remote Site Monitor (RSM), you will use a variety of tools and technologies to review study data. You will interact with study sites via phone, supporting the site teams and monitoring subject enrollment for the study. As a RSM you embody ethical research and business conduct, ensuring we never compromise quality or patient safety.
Grow within the RSM career path as a Senior or Principal RSM, develop into a Clinical Research Associate, or move into other roles or departments within Global Clinical Development.
Responsibilities:
Performs remote site management activities on assigned project(s) in accordance with FDA and/or local regulations and guidelines, ICH GCPs and PPD procedural documents.
Reviews study data from various sources remotely.
Contacts study sites to collect study documentation, resolves issues and requests outstanding information.
At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. It’s not just talk – our award winning training programs speak for themselves.
To learn how PPD can advance your career, apply now!
What To Expect NextWe look forward to receiving your application. A member of our talent acquisition team will review your qualifications and if interested, you will be contacted for an interview.
PPD is a leading global contract research organization. At PPD we are passionate, deliberate, and driven by our purpose – to improve health.
Remote Site Monitoring and Management (RSMM) blends on and off-site monitoring functions, providing efficiency to our clients. The RSMM group provides global time zone coverage and optimizes technology. Working in the RSMM group, you will contribute directly to PPD’s strategy to bend the time and cost curve of drug development by providing adaptive and intelligent monitoring services to our clients.
As a Remote Site Monitor (RSM), you will use a variety of tools and technologies to review study data. You will interact with study sites via phone, supporting the site teams and monitoring subject enrollment for the study. As a RSM you embody ethical research and business conduct, ensuring we never compromise quality or patient safety.
Grow within the RSM career path as a Senior or Principal RSM, develop into a Clinical Research Associate, or move into other roles or departments within Global Clinical Development.
Responsibilities:
Performs remote site management activities on assigned project(s) in accordance with FDA and/or local regulations and guidelines, ICH GCPs and PPD procedural documents.
Reviews study data from various sources remotely.
Contacts study sites to collect study documentation, resolves issues and requests outstanding information.
At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. It’s not just talk – our award winning training programs speak for themselves.
To learn how PPD can advance your career, apply now!
What To Expect NextWe look forward to receiving your application. A member of our talent acquisition team will review your qualifications and if interested, you will be contacted for an interview.
Qualifications
Education and Experience:Bachelor’s Degree in a life science-related field or relevant/equivalent combination of education, training and experience that provides the individual with the required knowledge, skills, and abilities.Knowledge, Skills and Abilities:Basic medical/therapeutic area knowledge and understanding of medical terminologyAbility to attain and maintain a working knowledge of FDA and/or local regulation and guidelines, ICH GCPs and PPD procedural documentsAbility to successfully complete PPD’s Clinical Foundation Training Program (CFP)Ability to evaluate medical research dataAbility to advise, counsel, and motivate investigational sitesEffective oral and written communication skills with the ability to communicate effectively with medical personnelExcellent interpersonal and customer service skillsGood organizational and time management skillsProven flexibility and adaptabilityStrong attention to detailAbility to work in a team or independently, as requiredGood computer skills with good knowledge of MS Office (Word, Excel, PowerPoint) and the ability to learn appropriate softwareAbility to extract pertinent information from all study documents, such as protocols, electronic study data systems, CTMS and dashboardExcellent English language and grammar skillsPPD 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 mannerAble to work upright and stationary for typical working hoursAbility to use and learn standard office equipment and technology with proficiencyAble to perform successfully under pressure while prioritizing and handling multiple projects or activitiesMay require travel (Recruiter will provide more details)
Qualifications
Education and Experience:Bachelor’s Degree in a life science-related field or relevant/equivalent combination of education, training and experience that provides the individual with the required knowledge, skills, and abilities.Knowledge, Skills and Abilities:Basic medical/therapeutic area knowledge and understanding of medical terminologyAbility to attain and maintain a working knowledge of FDA and/or local regulation and guidelines, ICH GCPs and PPD procedural documentsAbility to successfully complete PPD’s Clinical Foundation Training Program (CFP)Ability to evaluate medical research dataAbility to advise, counsel, and motivate investigational sitesEffective oral and written communication skills with the ability to communicate effectively with medical personnelExcellent interpersonal and customer service skillsGood organizational and time management skillsProven flexibility and adaptabilityStrong attention to detailAbility to work in a team or independently, as requiredGood computer skills with good knowledge of MS Office (Word, Excel, PowerPoint) and the ability to learn appropriate softwareAbility to extract pertinent information from all study documents, such as protocols, electronic study data systems, CTMS and dashboardExcellent English language and grammar skillsPPD 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 mannerAble to work upright and stationary for typical working hoursAbility to use and learn standard office equipment and technology with proficiencyAble to perform successfully under pressure while prioritizing and handling multiple projects or activitiesMay require travel (Recruiter will provide more details)