Clinical Project Manager - Pharmaceutical Trials

Placements24; O Mente; Híbrido; EUR 48.000 - 70.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health benefits

Retirement fund contributions

Hybrid work model

Career development opportunities

Descripción de la vacante

Placements24 is helping a leading pharmaceutical research organization fill the role of Clinical Project Manager to oversee pivotal multi-site trials from Queenstown, Eastern Cape hub. You will ensure adherence to GCP, ICH, and regulatory standards while coordinating study teams, sites, and vendors.

The ideal candidate has 5+ years in clinical research, strong leadership and budgeting skills, and proficiency with CTMS/EDC.

Formación

• Requires a life sciences degree with relevant clinical research knowledge.
• 5+ years in clinical research; at least 3 years in project management.
• Strong knowledge of GCP/ICH and regulatory requirements.

Responsabilidades

• Lead and oversee planning, execution, and monitoring of clinical trials per GCP/ICH.
• Select, train, and oversee clinical sites and investigators.
• Develop and manage study budgets and financial reporting.
• Create and manage project timelines and milestones.
• Ensure data integrity and quality of trial data.
• Manage relationships with CROs and central labs.
• Oversee recruitment and retention of participants.
• Prepare progress reports for stakeholders and regulators.
• Identify risks and mitigate issues impacting timelines.
• Ensure ethical and regulatory compliance throughout the trial lifecycle.

Conocimientos

Leadership

Communication

Interpersonal skills

CTMS experience

EDC systems

Organizational skills

Problem-solving

Multi-project management

English fluency

Educación

Bachelor's degree in life sciences

Advanced degree (Masters/PhD)

Herramientas

CTMS

EDC

Descripción del empleo

About the Role

Our client, a leading pharmaceutical research organization, is seeking a dedicated Clinical Project Manager to oversee vital clinical trials from their Queenstown, Eastern Cape hub. This critical role involves managing all operational aspects of clinical studies, ensuring adherence to regulatory requirements, ethical standards, and project timelines. The successful candidate will be instrumental in bringing life‑changing therapies to market by expertly managing research sites, study teams, and data integrity. This is an excellent opportunity to contribute significantly to healthcare innovation within the Eastern Cape and beyond.

Key Responsibilities

• Lead and manage the planning, execution, and monitoring of clinical trials in accordance with GCP, ICH guidelines, and regulatory requirements.
• Select, train, and oversee clinical trial sites and investigators.
• Develop and manage study budgets, ensuring cost‑effectiveness and timely financial reporting.
• Create and manage project timelines, ensuring milestones are met.
• Ensure the quality and integrity of clinical trial data collected.
• Manage relationships with external vendors, including CROs and central labs.
• Oversee the recruitment and retention of trial participants.
• Prepare and present regular progress reports to internal stakeholders and regulatory bodies.
• Identify and mitigate risks and issues that may impact trial conduct or timelines.
• Ensure compliance with all ethical and regulatory standards throughout the trial lifecycle.

Requirements

• A Bachelor's degree in a life science, nursing, pharmacy, or a related field.
• Advanced degree (Masters, PhD) is a plus.
• A minimum of 5 years of experience in clinical research, with at least 3 years in clinical project management.
• In‑depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
• Proven experience in managing clinical trial operations, including site management and monitoring.
• Strong leadership, communication, and interpersonal skills.
• Experience with clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Excellent organizational and problem‑solving abilities.
• Ability to manage multiple projects concurrently and prioritise effectively.
• Fluency in English; knowledge of other relevant languages is beneficial.
• Must be based in or willing to relocate to Queenstown, Eastern Cape , with a hybrid work arrangement.

Benefits

Our client offers a competitive salary, excellent health and wellness benefits, retirement fund contributions, and ample opportunities for professional development and career advancement within the pharmaceutical sector. The hybrid work model provides flexibility, balancing remote work with essential on‑site collaboration in Queenstown. Employees contribute to impactful research that improves global health outcomes and are part of a respected organization committed to scientific excellence. This role offers a chance to make a tangible difference in patient lives.