Training Development Lead, Associate Director, South Africa (Remote) - Fsp

Findojobs South Africa; South Africa; Remote; ZAR 1,200,000 - 1,800,000; Full time

Job summary

A leading clinical research organization in South Africa is seeking an experienced Training Development Lead, Associate Director. This role focuses on developing and overseeing global training courses in clinical research and regulatory areas. The ideal candidate should have a strong background in project management and instructional design, with at least 7 years in the pharmaceutical industry. This position offers opportunities for career development in a supportive work environment.

Benefits

Open and friendly work environment

Long-term career development opportunities

Qualifications

• 7+ years in the pharmaceutical industry focusing on pharmacovigilance, regulatory, and clinical.
• Expertise in training development and project management.
• Proficiency in LMS administration and various software tools.

Responsibilities

• Manage courseware development including design and deployment.
• Ensure project commitments are met through effective management.
• Partner with SMEs to develop and deploy training programs.
• Monitor training programs for compliance and effectiveness.
• Mentor junior colleagues and provide guidance.

Skills

Knowledge of adult learning principles

Instructional design

Project management

Clinical Research & Development knowledge

Negotiation skills

Education

BS with 7 years in pharmaceutical industry

MS with 5 years in pharmaceutical industry

Ph.D./PharmD/MD with 3 years in pharmaceutical industry

Tools

Microsoft Office

Adobe Acrobat

SharePoint

Articulate

Storyline

Job description

When our values align, there's no limit to what we can achieve.

Parexel is currently seeking a Training Development Lead, Associate Director to join us in South Africa, dedicated to a single sponsor.

This role will be responsible for providing strong technical expertise and training course development skills for the development and implementation of global training and educational courses in support of clinical research, medical, safety, and regulatory areas.

This position requires extensive instructional design, development, and project management skills, as well as the ability to work with stakeholders to establish development plans for key training and courses. Prior experience with the design, development, and implementation of quality global educational courses, advanced learning program management, and strong technical and communication skills are essential.

The scope of the role includes overseeing the overall educational program and training development, ensuring development plans utilize diverse and innovative methodologies for delivery and are produced with high quality to support Inspection Readiness.

Working as a Training Development Lead, Associate Director at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including leading global biotechs and Pharma top 50, with an incredible pipeline of work.

Expect exciting professional challenges in inspiring studies, balanced with time for your outside life.

Responsibilities

1. Manage courseware development, including course design, publishing, testing, and deployment.
2. Provide technical, instructional design, and operational management for programs, ensuring project commitments are met.
3. Communicate and ensure a global understanding of training strategy and goals.
4. Manage deliverables according to plans and timelines across multi-functional teams, including course design, development, and deployment.
5. Partner with business lines and Subject Matter Experts (SMEs) to identify training needs and develop/deploy training programs.
6. Develop processes and monitor activities related to compliance oversight of training programs; evaluate programs for effectiveness and customer satisfaction, utilizing feedback for continuous improvement.
7. Develop metrics, performance measures, reporting, and analysis to meet business and regulatory requirements; manage budgets for training projects.
8. Ensure compliance with training and education regulatory requirements and implement best practices globally to support inspection readiness.
9. Coordinate with sponsor learning groups to utilize existing educational resources and infrastructure.
10. Mentor junior colleagues and serve as a role model.

Requirements

Education: BS with 7 years in pharmaceutical industry focusing on pharmacovigilance, regulatory, and clinical OR MS with 5 years OR Ph.D./PharmD/MD with 3 years in the same focus areas.

Skills and Experience:

• Knowledge of adult learning principles, instructional design, development, and project management.
• Advanced knowledge of Clinical Research & Development, Pharmacovigilance, and/or Regulatory in pharmaceuticals.
• Ability to manage multiple complex projects concurrently.
• Experience monitoring adherence to compliance-based training programs.
• Effective influencing and negotiation skills.
• Ability to implement large-scale changes in complex, matrix organizations.
• Proficiency in LMS administration, Microsoft Office, Adobe Acrobat, SharePoint, Articulate, Storyline, and survey tools.
• Experience working with global teams and organizations.

We care about our people and your passion, as they are key to our success. We provide an open and friendly work environment with opportunities for long-term career development and skill enhancement within Parexel.

Who are Parexel

Parexel supports clinical studies across various therapeutic areas, with longstanding partnerships with a vast client base. We have supported trials for most of today’s top 50 best-selling drugs and enable niche developments critical to patient well-being.

You’ll be an influential member of the wider team.