Senior Clinical Research Associate

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Primary Location USA
Job ID: USA_SER_QAS-1224
Job Type: Full-Time

JOB DESCRIPTION

Your main responsibilities:

  • Perform site visits and monitoring activities in accordance with protocol, SOPs, GCP/ICH;
  • Participate in study site selection, including on-site and remote (by phone) pre-study site evaluation visits and feasibility assessment activities;
  • Conduct monitoring activities, including on-site and remote monitoring visits and in-house monitoring activities between visits;
  • Assist in developing patient enrollment strategies with the project team and study sites;
  • Collaborate with and coordinate site investigators ensuring overall integrity of study and adherence to guidelines, protocol and regulations;
  • Perform and assist with project-specific administrative activities as a member of the project team.

You have:

  • At least 6 years of CRA experience.  
  • Knowledge of ICH-GCP and national regulations related to clinical trials. 
  • Computer literacy: proficient MS Office user, knowledge of clinical trials’ related systems (CTMS, EDC, etc). 
  • Good to excellent organizational, record retention, decision making, customer service, communication and leadership skills. 
  • Combination of skills, knowledge and experience allowing to be a prominent team member with high potential for managing role.  
  • Ability to be assertive and work independently without direct supervision as well as in a team environment. 
  • Ability to work in bigger multi-country international clinical trials. 
  • Ability to establish and meet priorities, deadlines, and objectives. 
  • Focus on quality, precision, and timely delivery of results.

We offer:

  • Competitive salary and benefits;
  • Annual bonus scheme;
  • Flexible working arrangements;
  • Career opportunities at local, regional and global levels;
  • Support for personal and professional development (trainings, coaching, career development, international assignments, etc).

We provide equal opportunity to all qualified applicants and employees by prohibiting discrimination in employment decisions because of race, color, religion, sex, national origin, age, veteran status or disability.

If you are ready to start your journey at Cromos Pharma, please send your CV to cv@cromospharma.com.

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Cromos Pharma is an international contract research organization delivering integrated clinical research solutions that accelerate drug development.

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