Clinical Monitoring Analyst
4 weeks ago
This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication and organisation skills. Having experience with SAS programming is necessary. This role is part of a sponsor dedicated project where you will be working with the client directly to manage deliveries. The CMA contributes to the execution of the Centralized Monitoring process by performing the setup, programming and refresh(es) of the Centralized Monitoring platform, according to the study-specific Centralized Monitoring Plan (CMP). Main responsibilities Supports the Centralized Monitoring Lead (CML) in the development of the fit-for purpose CM strategy by contributing to the identification of the relevant CM elements to be implemented for the study (Quality Tolerance Limits (QTL), Key Risk Indicators, data visualizations and Data Quality Assessments) Setup/Program QTL, KRI and Data Quality Assessments according to the study CMP Refresh the Centralized Monitoring Platform at predefined frequency to enable signal identification Generate and maintain the Centralized Monitoring Platform specifications document and file it in eTMF Review and understanding of protocol is key Understand the data sources for the study, the data transfer specifications and the data structure Execute and document peer-review of CM platform setup done by other CMA colleagues Experience At least 3 years relevant experience in the area of pharmaceutical research and development or related field preferably in centralized Monitoring, data management, and/or biostatistics 2-3 years SAS experience including macro language Knowledge/ experience working on Cluepoints Ability to work in an autonomous way and engage with relevant stakeholders to execute activities related to study level centralized monitoring process. Ability to understand basic statistical analysis concepts and to interpret their outcome. Ability to maintain confidentiality of data and information during interactions with staff at all levels Ability to work with limited close supervision. Demonstrated communication, interpersonal, organizational and problem-solving skills High levels of initiative, drive and commitment. Prior experience in a Data Management related field is required Experience with relational databases, preferably Clinical Data Management and EDC Systems Experience communicating with all levels of personnel and participating in collaborative work team (locally and globally). Advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices. Excellent command, both verbal and written, of English This role is not eligible for UK visa sponsorship IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at #J-18808-Ljbffr
-
Clinical Monitoring Analyst
4 weeks ago
WorkFromHome, South Africa IQVIA Full timeClinical Monitoring Analyst (Cluepoints) - Remote Join to apply for the Clinical Monitoring Analyst (Cluepoints) - Remote role at IQVIA . This unique role within IQVIA is for a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication and organisational skills. Experience with SAS programming is necessary. The CMA is...
-
Clinical Monitoring Analyst
1 week ago
WorkFromHome, South Africa Iqvia Full timeClinical Monitoring Analyst (Cluepoints) - Remote Join to apply for the Clinical Monitoring Analyst (Cluepoints) - Remote role at IQVIA. This unique role within IQVIA is for a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication and organisational skills. Experience with SAS programming is necessary. The CMA is...
-
Clinical Monitoring Analyst
4 weeks ago
WorkFromHome, South Africa IQVIA Full timeClinical Monitoring Analyst (Cluepoints) - Remote IQVIA, Bloemfontein, Free State, South Africa This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication and organisation skills. Having experience with SAS programming is necessary. The CMA contributes to the execution...
-
Clinical Monitoring Analyst
3 weeks ago
WorkFromHome, South Africa IQVIA Full timeThis unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication and organisation skills. Having experience with SAS programming is necessary. This role is part of a sponsor dedicated project where you will be working with the client directly to manage deliveries. The CMA...
-
Remote Centralized Monitoring Analyst – SAS
1 week ago
WorkFromHome, South Africa Iqvia Full timeA leading global provider of clinical research services is seeking a skilled Clinical Monitoring Analyst for a remote role. The ideal candidate should have at least 3 years of experience in pharmaceutical research, strong SAS programming skills, and the ability to work autonomously while engaging with stakeholders. Responsibilities include supporting the...
-
WorkFromHome, South Africa IQVIA Full timeA global provider of clinical research services is seeking a Clinical Monitoring Analyst (Remote) to manage centralized monitoring strategies. The ideal candidate should have at least 3 years of relevant experience in pharmaceutical research with strong SAS programming skills. Responsibilities include supporting the Centralized Monitoring Lead and...
-
Remote Centralized Monitoring Analyst
4 weeks ago
WorkFromHome, South Africa IQVIA Full timeA leading global healthcare provider is seeking a Clinical Monitoring Analyst to contribute to the Centralized Monitoring process. Responsibilities include programming QTL and Data Quality Assessments, executing monitoring activities, and ensuring data confidentiality. Ideal candidates will have at least 3 years of experience in pharmaceutical research and...
-
Senior Clinical Data Analyst
2 weeks ago
WorkFromHome, South Africa Medium Full timeA leading healthcare data management firm is seeking a Senior Clinical Data Analyst based in South Africa. The role involves overseeing data management for complex clinical studies, mentoring junior staff, and ensuring compliance with regulatory standards. Candidates should have 5–8 years of industry experience, strong leadership abilities, and proficiency...
-
Senior Clinical Data Analyst
1 week ago
WorkFromHome, South Africa Parexel Full timeSenior Clinical Data Analyst (Home-based) – South Africa, Poland, Hungary or UK – FSP Join to apply for the Senior Clinical Data Analyst (Home-based) role at Parexel. Parexel is seeking a Senior Clinical Data Analyst to support commercial and development projects worldwide, joining a multi‑disciplinary team to plan and execute Data Management tasks for...
-
Senior Clinical Data Analyst — Remote Lead, EDC
3 weeks ago
WorkFromHome, South Africa Parexel International Full timeA leading clinical research organization is seeking a Senior Clinical Data Analyst to support international clinical studies. This fully remote role involves managing data management activities and leading a multi-disciplinary team. Requires a Bachelor's degree, 5-8 years in the industry, and strong English communication skills. You will mentor staff and...
