Clinical Study Manager

Choosing the right company when looking for your next role can be a challenge. We partner with a select few Medical affairs, Access and Evidence organisations to match candidates with the correct company, perfectly matching your values, goals and work like balance needs with our partners.

We partner with Medical organisations that have people at its centre, share our passion for collaboration and ongoing training and development programmes.

So whether you're looking to work within an office, remote or have niche requirements we'll help you select the right agency to allow you to thrive in and out of work.

You'll thrive if you:

• Collaborate with Global Clinical Trial Manager(s) to ensure country level study delivery is aligned with the global study project plan
• Ensure implementation of study(ies) in accordance with SOPs and ICH/GCP guidelines
• Ensure relevant systems are updated to enable accurate reporting of study progress and milestone deliverables
• Contribute to development of study-specific materials e.g. monitoring plan, study specific training documents
• Ensure regional, country and site vendor set-up, conduct and quality e.g. laboratories and equipment provisioning
• Support audit and inspection activities and contribute to CAPAs, including leading resolution of issues when appropriate
• Support and contributing to Clinical Study Team(s)
• Have the ability to use scientific and clinical knowledge to conceptualize study designs

What our partner's like to see:

• Project planning experience including oversight of study deliverables, budgets, and timelines
• Experience writing and presenting clearly on scientific and clinical issues
• Working knowledge of International Conference on Harmonization (ICH), Good Clinical Practice (GCP), and applicable international regulations and guidelines
• Knowledge of project risk management assessment and mitigation approaches
• Experience in working with external clinical research vendors (CROs, central labs, imaging vendors, etc.)
• Experience in life sciences or medically related field, with ideally at least 4 years clinical research experience obtained working on clinical trials either within a biotech, pharmaceutical or CRO company

Apply now and let's have a conversation all about you, so we can find your perfect next role.

#CRO #Clinicalresearch #biotech #clinicaltrials #Pharmaceutical #imaging #lifescience #ClinicalStudyManager