Clinical Team Manager - Contractor (Spanish Speaking)

Posted 2 Days Ago
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Hiring Remotely in Mississauga, ON, CAN
In-Office or Remote
Mid level
Biotech • Pharmaceutical
The Role
The Clinical Team Manager oversees operational project management, ensuring project team training, developing project documents, and initiating corrective measures in clinical trials.
Summary Generated by Built In
Company Description

Ergomed PLC 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., 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.  

Skills Required

  • Extensive clinical research lead experience in multiple studies
  • Experience in managing Clinical part of studies in more than one region
  • Experience of phase 2/3 trials, ideally complex studies such as oncology or rare disease
  • A minimum of a science-based bachelor's degree
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The Company
HQ: Raleigh, NC
535 Employees
Year Founded: 1997

What We Do

Founded in 1997, Ergomed is a global provider of high-quality services to the biopharmaceutical industry, spanning all phases of clinical trials, post-approval pharmacovigilance, and medical information. Ergomed’s fast-growing services business includes an industry-leading suite of specialist pharmacovigilance (PV) solutions, integrated under the PrimeVigilance brand, and Ergomed Clinical Research, a complete, global Phase I-IV clinical development and trial management services with a strong heritage in the development of drugs in rare diseases and oncology. • 1,400+ highly qualified professionals • Global full-service CRO • 25+ years of experience • Therapeutic specialization in oncology • Strong expertise in rare disease trials • Robust clinical safety system • Choice of leading drug safety databases Our key services include: • Clinical Research Services • Pharmacovigilance • Medical Information • Regulatory • Medical Writing • Site Management • Study Physician Support • Biostatistics • Patient Study Support

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