Senior / Clinical Research Associate

Proclinical is currently recruiting for a remote Senior/Clinical Research Associate for a global provider of drug development solutions. As the Senior Clinical Research Associate, you will work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - III, ensuring adherence to applicable regulations and principles of ICH-GCP.

Job Responsibilities:

• Working independently and proactively to coordinate all necessary activities required to set up and monitor a study, completing accurate study status reports and maintaining study documentation
• Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested
• Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required
• Managing sponsor generated queries efficiently and responsible for study cost effectiveness
• Dependent on level of experience you may assist in training and mentoring less experienced CRA's and/or manage CRA's working on international projects

Skills and Requirements:

• Minimum of 3 years of active independent field monitoring experience- all types of visits.
• Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
• Excellent communication and interpersonal skills, both written and verbal enabling you to deal with queries in a timely manner
• Ability to produce accurate work to tight deadlines within a pressurized environment

If you are having difficulty in applying or if you have any questions, please contact Polina Sidorova at p.sidorova@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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