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Clinical Team Manager

Role overview

Qualifications

  • Extensive clinical research lead experience in multiple studies
  • Experience in managing Clinical part of studies in more than one region or equivalent study complexities
  • Experience of phase 2/3 trials, ideally complex studies such as oncology or rare disease
  • A minimum of a science-based bachelor’s degree

Responsibilities

  • Responsible for operational project management
  • Proactively identifies, resolves/mitigates, and escalates risks and/or issues
  • Verifying and ensuring that project team members are trained
  • Developing, reviewing and revision of project documents

Key facts

Other skills

  • Training And Development
  • Communication
  • Problem Solving

About the company

PrimeVigilance logo

PrimeVigilance

Contract Research Organizations (CRO)

PrimeVigilance, an Ergomed company, was set up by former Pharmacovigilance Regulators in 2008. We have grown to become the leading Pharmacovigilance specialist company, delivering global solutions for both clinical safety and post-marketing pharmacovigilance, as well as medical information from our offices. Having successfully delivered Pharmacovigilance (PV) and Medical Information (MI) services for over 14 years, our experience enables us to offer a comprehensive, top quality, cost-effective, and innovative safety solution. Our flexible approach, tailor-made to work with clients, allows us to deliver the services that meet your clinical and post-marketing needs.From its operational hubs based in Europe, the USA, and Japan. PrimeVigilance manages a global Pharmacovigilance system with a choice of leading drug safety databases, stretching to more than 100 countries.• 900+ highly qualified professionals• Global leader in QPPV services• 24/7 multilingual call center• Choice of leading drug safety databases• Robotic Process Automation (RPA) expertise• Access to regulatory experts and key opinion leadersGLOBAL LIFE CYCLE MANAGEMENT SERVICES• PHARMACOVIGILANCE • PHARMACOEPIDEMIOLOGY & BENEFIT-RISK MANAGEMENT• AUDIT & INSPECTION• QUALITY MANAGEMENT• REGULATORY SCIENCE

Company details

IndustryContract Research Organizations (CRO)
Company size501 - 1000

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Job description

Company Description

Ergomed is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease.   

Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America, and Asia. 

Our company allows for employee visibility (you have a voice!) creative contribution and realistic career development.   

We have nourished a true international culture here at Ergomed.   

We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved.  

Come and join us in this exciting journey to make a positive impact in patient’s lives.   

Job Description

     Responsibilities: 

  • The Clinical Team Manager will be responsible for operational project management 

  • The CTM proactively identifies, resolves/mitigates, and escalates risks and/or issues to the PM/PD and Head of Clinical Operations as necessary 

  • Verifying and ensuring that project team members (CRAs, Site Managers, CTAs) are trained (e.g., GCP, SOP, indication, protocol, study specific procedures / requirements, etc.) to perform their assignments 

  • Developing, reviewing and revision of project documents (e.g., clinical monitoring plan, CRF completion guidelines, study specific operating manual, study specific forms etc.)   

  • Initiating corrective / preventative measures – e.g., update of study guidance documents, performing re-training, performing co-monitoring, etc. 

 

Qualifications

 

  • Extensive clinical research lead experience in multiple studies  

  • Experience in managing Clinical part of studies in more than one region or equivalent study complexities 

  • Experience of phase 2/3 trials, ideally complex studies such as oncology or rare disease 

  • Able to work in a fast-paced small CRO environment and manage multiple projects 

  • A minimum of a science-based bachelor’s degree 

  • Able to work effectively with minimal supervision 

 

 

Additional Information

Why Ergomed   

We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.   

To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us.  

We offer:  

  • Training and career development opportunities internally   

  • Strong emphasis on personal and professional growth  

  • Friendly, supportive working environment  

  • Opportunity to work with colleagues based all over the world, with English as the company language  

Our core values are key to how we operate, and if you feel they resonate with you then Ergomed is a great company to join!   

  • Quality  

  • Integrity & Trust   

  • Drive & Passion   

  • Agility & Responsiveness   

  • Belonging  

  • Collaborative Partnerships   

We look forward to welcoming your application.  

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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