Clinical Trials Assistant Peterborough

Clinical Research Assistant / Clinical Trial Assistant, Peterborough

Monday – Friday, daytime hours, site based (22.5 hours per week, flexible to suit you)                                                                                                                        

6 month contract

Are you looking for your next opportunity in Clinical Research?  Do you want to work for an industry leading company that offers you an excellent benefits package and supports career progression?  If so, come and join us - IQVIA are looking for an experienced site-based Clinical Research Assistant in Peterborough.

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.

Day to day responsibilities will include:

• Verifying and/or correcting research study information on source documents; researching queries and variances; providing feedback to the site data collector Accurate input of trial data into the Electronic Data Capture (EDC) system Preparing / maintaining study files, and submission of information according to deadlines Collecting / submitting and assisting in maintaining relevant regulatory and ethics documentation Scheduling visits with research subjects and generating appropriate reports and documentation Tracking patient visits and procedures completed against the study budget by inputting data into the clinical trial management system (CTMS) Processing lab specimens including labelling of vials and accurately filling out requisitions for storage and/or shipment per the study protocol and shipment regulations Performing other administrative support functions such as reception, office organization, and office supply management.

We are looking for candidates with the following skills and experience:

• BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession  Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules Basic knowledge of medical terminology Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clients Good organisational skills with the ability to pay close attention to detail.