Clinical Trial Project Manager – 2-Year Fixed Term

Ajpersonnel; Durban; On-site; ZAR 200 000 - 300 000; Full time

Job summary

A leading clinical research organization in Durban is seeking a qualified individual for a fixed-term contract position focused on project management in clinical trials. Applicants should hold a Master's in relevant sciences and possess strong organizational skills, attention to detail, and the ability to manage multiple priorities. The role involves coordinating research activities, meeting stakeholders, and maintaining adherence to project timelines. Ideal candidates should be proficient in MS Office and have experience in clinical trials.

Qualifications

• Must have clinical trial conduct experience and previous project management experience.
• ICH (R3) and SA GCP certification are mandatory.
• Computer literacy with advanced skills in MS Office and Project is required.

Responsibilities

• Coordinate VM-CTU activities as per unit milestones and timelines.
• Organize meetings with various stakeholders and distribute summaries.
• Provide secretariat support for JSC PSRT DSMB.
• Ensure secure storage and curation of scientific data.
• Report writing as per funder requirements.
• Offer science presentation and medical writing support.

Skills

Revenue Cycle Management

HIPAA

Healthcare Management

PMBOK

Microsoft Outlook

Project Leadership

Data Management

Project Management

Affiliate Marketing

Project Management Software

Supervising Experience

Workday

Education

Masters Degree in Science Immunology Medicine Microbiology Public Health or Associated Allied Health Professions

Tools

MS Office

MS Project

eTMF or eISF software

Job description

A leading clinical research organization in Durban is seeking a qualified individual for a fixed-term contract position focused on project management in clinical trials. Applicants should hold a Master's in relevant sciences and possess strong organizational skills, attention to detail, and the ability to manage multiple priorities. The role involves coordinating research activities, meeting stakeholders, and maintaining adherence to project timelines. Ideal candidates should be proficient in MS Office and have experience in clinical trials.