FSP-CRA II

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.

Essential Job Duties: 
1) The below statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties. 
2) Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned 
3) Responsible for all aspects of site management as prescribed in the project plans 
4) General On-Site Monitoring Responsibilities: 
5) Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study 
6) Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements 
7) Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review 
8) Monitor data for missing or implausible data 
9) 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 travel policy 
10) Ensure audit readiness at the site level 
11) Travel, including air travel, may be required and is an essential function of the job. 
12) Prepare accurate and timely trip reports 
13) Manage small projects under direction of a Project Manager/Director as assigned 
14) Serve as lead monitor for a protocol or project, and may assist in establishing monitoring plans and trip report review as assigned 
15) Review progress of projects and initiate appropriate actions to achieve target objectives 
16) Organize and make presentations at Investigator Meetings 
17) Participate in the development of protocols and Case Report Forms as assigned 
18) Participate in writing clinical trial reports as assigned 
19) Interact with internal work groups to evaluate needs, resources and timelines 
20) Act as contact for clinical trial supplies and other suppliers (vendors) as assigned 
21) Responsible for all aspects of registry management as prescribed in the project plans 
22) Undertake feasibility work when requested 
23) Conduct, report and follow-up on Quality Control (QC) visits when requested 
24) 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 
25) Negotiate study budgets with potential investigators and assist the Fortrea legal department with statements of agreements as assigned 
26) Track and follow-up on Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs 
27) Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management 
28) Assist with training, mentoring and development of new employees, e.g. co-monitoring 
29) Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client contact as assigned 
30) Perform other duties as assigned by management 
Minimum Required: 
• Three-Four (3-4) years of Clinical Monitoring experience 
• Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs 
• Advanced site monitoring skills 
• Advanced study site management skills 
• Advanced registry administration skills 
• Ability to work with minimal supervision 
• Good planning and organization skills 
• Good computer skills with good working knowledge of a range of computer packages 
• Advanced verbal and written communication skills 
• Ability to train and supervise junior staff 
• Ability to resolve project-related problems and prioritizes workload for self and team 
• Ability to work within a project team 
• Works efficiently and effectively in a matrix environment 
• University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure) 
• In lieu of the above education requirement, candidates with a minimum of 6 years recent clinical monitoring experience will be considered 
• Thorough knowledge of regulatory requirements 
• Thorough understanding of the drug development process 
• Fluent in local office language and in English, both written and verbal 
•Or an equivalent combination of education and experience to successfully perform the key responsibilities of the job
 

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.