As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

Our Flexible Solutions Clinical Research Associates are based at our pharmaceutical client sites and manage all aspects of study site monitoring according to Client SOP, GCP, and ICH guidelines, including pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and maintenance of study files.

Responsibilities include:

•Responsible for all aspects of study site monitoring including routine monitoring and closeout 
of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with 
vendors; and other duties, as assigned. 
• Responsible for all aspects of site management as prescribed in the project plans.
• General On-Site Monitoring Responsibilities.
• Ensure the study staff who will conduct the protocol have received the proper materials and 
instructions to safely enter patients into the study.
• Ensure the protection of study patients by verifying that informed consent procedures and 
protocol requirements are adhered to according to the applicable regulatory requirements.
• Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data 
collection tools by careful source document review.
• Monitor data for missing or implausible data.
• Ensure the resources of the Sponsor and Fortrea are spent wisely by performing the required 
monitoring tasks in an efficient manner, according to SOPs and established guidelines, 
including managing travel expenses in an economical fashion according to Fortrea or Sponsor travel 
policy.
• Ensure audit readiness at the site level.
• Travel, including air travel, may be required and is an essential function of the job. 

•Prepare accurate and timely trip reports.
• Interact with internal work groups to evaluate needs, resources, and timelines.
• Act as contact for clinical trial supplies and other suppliers (vendors) as assigned. 
• Responsible for all aspects of registry management as prescribed in the project plans. 
• Undertake feasibility work when requested. 
• Participate in and follow-up on Quality Control Visits (QC) when requested. 
• Recruitment of potential investigators, preparation of EC submissions, notifications to 
regulatory authorities, translation of study-related documentation, organization of meetings 
and other tasks as instructed by supervisor as assigned 18) Assist Senior CRA with managing 
investigator site budgets. 
• Track and follow-up on Serious Adverse Event (SAE) reporting, process production of reports, 
narratives and follow up of SAEs. 
• Independently perform CRF review; query generation and resolution against established data 
review guidelines on Fortrea or client data management systems as assigned by management. 
• Assist with training, mentoring and development of new employees, e.g., co-monitoring. 
• Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if 
applicable), and may act as a local client contact as assigned. 
• Perform other duties as assigned by management. 
 

Requirements

• At least 1-year full time work experience as CRA focus on drug trial.
• Able to conduct monitor daily works independently.
• Bachelor degree or above.
• Have basic sense of ICH-GCP. Have received at least one QC visit in responsible sites.
• Smart and quick to catch up. Have good capability in self-learning, communication and
  planning.
• Better to have experience in global pharmaceutical company studies
• Better to have strategic thinking and risk management sense.
• Be capable of working under high pressure
  Requirement on EN
• Listening-able to take EN training and meetings
• Speaking-able to communicate with EN speaking people clearly
• Reading-able to read EN protocol and academic materials
• Writing-able to write EN e-mails and reports