When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Parexel is currently registering interest for a Training Development Lead, Manager to join us in the UK, dedicated to a single sponsor, for a 12 month fixed-term contract position.
Previous experience of working in clinical trials L&D , or a good understanding of the clinical trial life-cycle from study start up through submission to the regulatory authorities is required.
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.
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 technical and communication skills are essential.
The scope of the role will cover the overall educational program and training development deployment and maintenance processes as needed, ensuring development plans utilise diverse and innovative methodologies for delivery and are produced with high quality in support of Inspection Readiness.
Working as a Training Development Lead, Manager at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work.
Expect exciting professional challenges in inspiring studies, but with time for your outside life.
Responsibilities
Manage courseware development including course design, publishing, testing and deployment.
Provide technical, instructional design and operational management for programs and be accountable for meeting project commitments.
Communicate and ensure a global understanding of training strategy and goals.
Manage deliverables according to endorsed plans and timelines across multi-functional teams including course design, development and deployment.
Partner with associated business line and Subject Matter Experts (SMEs) to proactively identify training needs and development and deployment of training programs.
Advised on processes, as needed, and monitor activities related to compliance oversight of training programs; ensure programs and projects are evaluated for effectiveness and customer satisfaction and that feedback is utilised as part of the continuous improvement process.
Development of metrics and performance measures, reporting and analysis to meet business needs, and regulatory requirements; budget management; develop and manage budget for training projects.
Ensure compliance with training and education regulatory requirements and consistent implementation of best practices, standards, and training globally to support inspection readiness.
Mentor junior colleagues and serve as a role model.
Here are a few requirements specific to this advertised role.
Education:
Bachelor’s degree.
MA in Ed Tech / Instructional Design is preferred.
Skills and experience:
Minimum of 1 year of pharmaceutical industry with focus on pharmacovigilance, regulatory and or clinical development.
Minimum of 5 years’ experience designing, developing, and delivering learning solutions.
Demonstrated knowledge of adult learning principles, and experience design.
Sound knowledge of Clinical Research & Development, Pharmacovigilance, and/or Regulatory in the pharmaceutical industry.
Demonstrated ability to manage multiple projects concurrently.
Preferably prior experience in monitoring adherence to compliance-based training programs.
Proficiency in Microsoft Office, Articulate suite, and at least one of the following: Adobe, Vyond, Camtasia, Storyline, Rise, , Synthesia, Well Said Labs, or Powtoons.
We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel.
Who are Parexel
Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.
We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.
You’ll be an influential member of the wider team.
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