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Senior Clinical Research Associate

Role overview

Qualifications

  • College/University degree in Life Sciences or equivalent
  • Extensive on-site monitoring experience in phase 2/3 trials, ideally in oncology or rare disease
  • Full working proficiency in English
  • Ability to plan, multitask and work in a dynamic team environment

Responsibilities

  • Perform on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities
  • Identify the investigators and verify their qualifications, resources, facilities, equipment and staff
  • Train investigational site staff as necessary
  • Participate in mentoring/training of new staff and conducting co-monitoring visits

Key facts

Other skills

  • Training And Development
  • Communication
  • Collaboration
  • Problem Solving
  • Planning
  • Multitasking
  • Teamwork

About the company

ERGOMED logo

ERGOMED

Pharmaceuticals

Ergomed’s fast-growing services business includes an industry-leading suite of specialist pharmacovigilance solutions, integrated under the PrimeVigilance brand and a full range of high-quality clinical research and trial management services under the Ergomed Clinical Research brand. The Ergomed group employs over 1,800 people and operates out of 24 offices around the world, providing its services to researchers and patients in around 100 countries globally. Our Ergomed Clinical Research business was founded in 1997 and provides high-quality clinical research and trial management services globally and across all trial phases (I to IV), specialising in oncology and rare disease trials. We use innovative site-support services which focus on enhancing patient recruitment and engagement, with a strong heritage in Europe and the USA. PrimeVigilance is a global leader in pharmacovigilance and specialised multi-lingual medical information services. Since 2008, the PrimeVigilance business has supported pharmaceutical, biotechnology and genetics companies in managing the global safety of their products, all the way from clinical trial to post-marketing. Our pharmacovigilance services include case processing, signal and risk management, pharmacoepidemiology, audits, training, advisory literature services, medical information and QPPV.

Company details

Company typeLarge
IndustryPharmaceuticals
Company size1001 - 5000

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Job description

Company Description

Ergomed Group 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

  • Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study 
  • Identifies the investigators and verifies that the investigator has adequate qualifications, resources, facilities, equipment and staff to conduct the clinical study throughout the study period. 
  • Trains investigational site staff as necessary 
  • When applicable, supports preparation of regulatory and / or EC submissions 
  • Participates in mentoring/training of new staff as well as performing co-monitoring visits, to assess junior staff performance. 

 

Qualifications

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience 
  • Extensive on-site monitoring experience in phase 2/3 trials, ideally with experience of complex trials in oncology or rare disease 
  • Full working proficiency in English 
  • Ability to plan, multitask and work in a dynamic team environment 
  • Communication, collaboration, and problem-solving skills 
  • Ability to travel nationally 

Additional Information

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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