Strategic Remote Leisure Facilities Manager

Placements24; Cape Town; Remote; ZAR 420,000 - 600,000; Full time

Benefits offered by this job

Health insurance

Annual leave

Life assurance

Retirement planning

Global EAP

Job summary

ICON Strategic Solutions is seeking a Central Review Coordinator in Cape Town. You will support a sponsor-dedicated model with centralized endpoint data evaluation and grading across multiple studies.

Key tasks include study trackers, reviewer assignments, data entry follow-up, and effective communication within project teams. Requires CRO/pharmaceutical experience, solid data management skills, and proficiency with Word/Excel.

Qualifications

• BSc Life Science degree with solid experience working within a CRO and or the pharmaceutical industry
• A genuine interest in using your clinical experience to develop your career in clinical data
• Strong experience with at least one of the data management systems i.e. Rave
• Experience in most study tasks
• Comfortable working within a project team and have excellent written and verbal communication skills
• Experience in Microsoft Word and Excel
• Strong attention to detail
• Effective time management and prioritization skills

Responsibilities

• Create and maintain Study Trackers.
• Monitor screening deadlines; follow up with sites on data entry and other vendor data entry and elevate any visits that are not released for CR review or where queries are not being addressed within the timelines.
• Review and determine on study visits and sweeps are ready for review using the page status and query reports.
• Create, send and process assignments to reviewers, including query tracking.
• Download and compile files for the patient profile creation and post on the Central Grading Portal for the Data Programmer, CRS.
• Create internal CRS agenda and meeting minutes for distribution
• Action/Decision log updates/maintenance
• Filing of documents in Central Grading Portal and eTMF.
• Liaise with Directors, Therapeutic Expertise, internal team members and Sponsors.
• Performs proficient reviews of study datasets prior to client transfer, if applicable.
• Monitor review progress to meet timelines, identify issues, risks, possible solutions & report to Lead Central Review Manager.
• Participates in database lock activities.
• Serve as CR Coordinator on more or more projects.

Skills

CRO experience

Data management systems

Communication skills

Time management

Team collaboration

Education

BSc Life Science degree

Tools

Rave

Job description

Central Review Coordinator

At ICON Strategic Solutions, you will work in a sponsor‑dedicated model, supported by ICON's global expertise. As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. This role as Central Review Coordinator offers the right candidate the opportunity to join the Central Review Services team; which is unique in the CRO industry. The team is solely focused on delivering independent, centralized endpoint data evaluation, grading, and data management for one of our Big Pharma FSPs. The central review process produces a higher level of accuracy and decreased variability that is essential in endpoint measurement and analysis.

Responsibilities

• Create and maintain Study Trackers.
• Monitor screening deadlines; follow up with sites on data entry and other vendor data entry and elevate any visits that are not released for CR review or where queries are not being addressed within the timelines.
• Review and determine on study visits and sweeps are ready for review using the page status and query reports.
• Create, send and process assignments to reviewers, including query tracking.
• Download and compile files for the patient profile creation and post on the Central Grading Portal for the Data Programmer, CRS.
• Create internal CRS agenda and meeting minutes for distribution
• Action/Decision log updates/maintenance
• Filing of documents in Central Grading Portal and eTMF.
• Liaise with Directors, Therapeutic Expertise, internal team members and Sponsors.
• Performs proficient reviews of study datasets prior to client transfer, if applicable.
• Monitor review progress to meet timelines, identify issues, risks, possible solutions & report to Lead Central Review Manager.
• Participates in database lock activities.
• Serve as CR Coordinator on more or more projects.

You will have/be

• BSc Life Science degree with solid experience working within a CRO and or the pharmaceutical industry
• A genuine interest in using your clinical experience to develop your career in clinical data
• Strong experience with at least one of the data management systems i.e. Rave
• Experience in most study tasks
• Comfortable working within a project team and have excellent written and verbal communication skills
• Experience in Microsoft Word and Excel
• Strong attention to detail
• Effective time management and prioritization skills

What ICON can offer you

• Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
• Competitive salary
• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family's needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.