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Associate Clinical Research Associate (trainee)

Wavre, Wallonia, Belgium Date posted 08/04/2020 Job ID post-50024425 b

Everything we do has the potential to impact patient lives, and our Clinical Research Associates (CRAs) take their work seriously, demonstrate empathy, and act with heart. They also perform with urgency, navigating our streamlined clinical operating model to drive effectiveness, reduce handoffs and increase employee, client and site satisfaction.

As a CRA at Parexel, you‘ll be joining a team with a wide variety of experiences and knowledge. We’re looking for people like you to take the initiative to do things better and smarter—people who want to grow personally and professionally. We recognize and uphold the importance of all people, the way we do things, our quest for innovation, and most importantly, our patients.

  • Full Time
  • Level: Mid
  • Travel: Yes
  • Glassdoor Rating 3.5

Success Profile

Check out the top traits we’re looking for and see if you have the right mix.

  • Innovative
  • Problem-Solver
  • Communicator
  • Tech-Savvy
  • Confident
  • Independent

"The harmonious environment at Parexel contributes to our success; the great collaboration helps to achieve the goals as one team, and to keep positivity, interest and development alive."

Nicla – Sr Clinical Research Associate
 

Rewards

  • Global Impact

    We are one truly global team working together to propel each client´s journey ahead faster.

  • Balance

    We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.

  • Collaboration

    Work with industry leaders and subject matter experts.

  • Freedom

    The ability to innovate, ask “what if” and try new solutions without fear of failure.

  • Variety

    Opportunities to work on multiple accounts – never boring!

  • Compensation

    Competitive salaries and bonus structure based on individual metrics.

Responsibilities

The Role for Associate Clinical Research Associate (aCRA) has been created in Parexel to train and develop people, without any experience in clinical research. During the training period (minimum 5 months), aCRA is responsible for learning and developing skills and competencies to work in a clinical research environment. At the end of this period the aCRA would be ready to work independently within Global Clinical Operations Department in Parexel


Key Accountabilities:

• Complete all mandatory trainings in our electronic Learning Management System
• Do all pre-work that applies to each training activity
• Complete and deliver on time all activities including post-training activities
• Attend all on-going, relevant trainings, including Continuing Education Workshops (CEW) that are applicable
• Attend all training activities organized for this role (in the country or at international level)
• Learn to work in compliance with ICH-GCP Guidelines, applicable international and local regulations, Parexel SOPs, other Parexel and study specific procedures and requirements
• Arrange on-site observational visits and logistics (e.g. travel arrangements).
• Perform on-site observational visits (Qualification, Initiation, Monitoring and Termination) with appropriate support; apply judgment and knowledge to independently resolve site issues,
Work with the mentor in the visit report and follow up letters writing activities.
• Successfully pass all assessments related to this role
• Complete routine departmental administrative tasks in a timely manner (e.g. times, metrics, concur etc.)
• Attend to all internal activities and corporate meetings.
• Perform project specific training agreed to understand the main project activities
• Ensure the basic understanding of project scope, milestones, budgets, and time codes and strive for high quality, timely, and induction period, shadow efficient delivery working in two or three.
• Help the local team in completing Clinical Trial Management defined trial
Systems (CTMS) and study specific trackers
• Track, scan, code and apply naming convention and send documents to the relevant study e-CF Work In Progress (WIP) area and Central File (CF) area of TMF as per the Central File Maintenance Plan, if applicable
• Filling and Archiving paper wet-ink documents in the Central Files office location as per the Central File Maintenance Plan (CFMP) if applicable
• Assist with the creation and completion of the Investigator Site File if applicable
• Support in on-site / remote visits preparation and follow-up if applicable

Qualifications

The Role for Associate Clinical Research Associate (aCRA) has been created in Parexel to train and develop people, without any experience in clinical research. During the training period (minimum 5 months), aCRA is responsible for learning and developing skills and competencies to work in a clinical research environment. At the end of this period the aCRA would be ready to work independently within Global Clinical Operations Department in Parexel


Key Accountabilities:

• Complete all mandatory trainings in our electronic Learning Management System
• Do all pre-work that applies to each training activity
• Complete and deliver on time all activities including post-training activities
• Attend all on-going, relevant trainings, including Continuing Education Workshops (CEW) that are applicable
• Attend all training activities organized for this role (in the country or at international level)
• Learn to work in compliance with ICH-GCP Guidelines, applicable international and local regulations, Parexel SOPs, other Parexel and study specific procedures and requirements
• Arrange on-site observational visits and logistics (e.g. travel arrangements).
• Perform on-site observational visits (Qualification, Initiation, Monitoring and Termination) with appropriate support; apply judgment and knowledge to independently resolve site issues,
Work with the mentor in the visit report and follow up letters writing activities.
• Successfully pass all assessments related to this role
• Complete routine departmental administrative tasks in a timely manner (e.g. times, metrics, concur etc.)
• Attend to all internal activities and corporate meetings.
• Perform project specific training agreed to understand the main project activities
• Ensure the basic understanding of project scope, milestones, budgets, and time codes and strive for high quality, timely, and induction period, shadow efficient delivery working in two or three.
• Help the local team in completing Clinical Trial Management defined trial
Systems (CTMS) and study specific trackers
• Track, scan, code and apply naming convention and send documents to the relevant study e-CF Work In Progress (WIP) area and Central File (CF) area of TMF as per the Central File Maintenance Plan, if applicable
• Filling and Archiving paper wet-ink documents in the Central Files office location as per the Central File Maintenance Plan (CFMP) if applicable
• Assist with the creation and completion of the Investigator Site File if applicable
• Support in on-site / remote visits preparation and follow-up if applicable

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