In House CRA

In House CRA -Location: Remote Remote RomaniaRemote Remote RomaniaJob Type: Regular Full-timeDivision: Precision for MedicineBusiness Unit: Clinical SolutionsRequisition Number: 5991Precision for Medicine is recruiting an In-House CRA to join our global team. Candidates can work remotely in Hungary, Poland, Romania, Serbia or Slovakia. Essential functions of the job include but are not limited to: Assist with the investigator recruitment activities utilizing phone scripts, questionnaires, study site materials and other tools for use in evaluating investigative sites. May assist in identifying study sites by performing site feasibility and recruitment tasks, e. g.

, completing, disseminating, and reviewing responses to site recruitment questionnaires. Schedules and attend internal and external meetings as required. Prepares Investigator Site Files including distribution to study sites (electronically or physically), coordination with shipping vendor, if required. Performs ongoing essential document collection and review, maintenance, and close-out activities, organizing and maintaining site level data in the trial master file (TMF) under general supervision ensuring that sponsor and investigator obligations are being met and are compliant with ICH/GCP guidelines and applicable local regulations. Assist with set ups and maintains site-related data in applicable clinical systems according to procedures and guidelines.

Utilizes the Clinical Trial Management System (CTMS) to ensure milestones and activities are accurately tracked. Acts as site contact/liaison for study and site management issues including addressing questions, assists with managing study supplies, and may support offsite central monitoring activities. Escalates issues and risks as needed. Ensures timely and complete data entry by site in EDC or any other system that requires data entry. Sends email blasts/newsletter, updates, and updated study core documents to study site personnel. Assists in providing logistics support in samples management and tracking, where applicable and in study supply management.

Supports investigators and investigative staff in fulfilling obligations regarding local submissions according to local regulatory and Institution Review Board (IRB)/Independent Ethics Committee (IEC) requirements. Assists in data review inclusive of site level data review, resolutions provided by sites to queries, facilitates database closure and freezing procedures as per study plans. Assist with study tracking via the CTMS, Study specific trackers or sponsor designated system to ensure that the study reporting is current, accurate and complete. Documents site and Sponsor contact and study interactions in a timely and professional manner.

Assist in remote review of the electronical Investigator Site File, where applicable. Assists with Investigational Product accountability, where applicable. Consults with project team members regarding study site issues. Provides quality review of the amended site level informed consent template. Follows up with sites for trial invoices and ensures the CTMS is accurately updated to allow the timely processing of Investigator Payments. May attend site visits as needed, supporting the CRA to ensure sponsor and investigator obligations related to the study documentation are being met and are compliant with applicable regulatory requirements and guidelines.

May serve as an Independent Essential Document Reviewer post-SIV. Supports on-site visits activities if needed. Performs other duties as assigned by management. Performs all tasks in accordance with applicable guidelines, (e. g. , ICH-GCP), company and sponsor SOPs, project plan, study-specific processes, local regulatory requirementsQualificationsMinimum Required:

Bachelor's degree / international equivalent or equivalent combination of education and experience ideally in a business, scientific or healthcare disciplineMinimum of 1 year experience working in the clinical trial industryeTMF experienceMust be fluent in the English languageOther RequiredHigh in proficiency in the Microsoft Office package of programs (Outlook, Word, Excel, and PowerPoint)Customer service demeanor; demonstrate flexibility and teamworkAbility to focus on detail for extended periods of time, high attention to accuracyWorking knowledge of the drug development processExcellent organizational skillsAbility to work efficiently in a remote work environmentAn additional language:

Spanish, French, Italian or German is desirable although not essentialCompetenciesGood knowledge and utilization of ICH-GCP, Precision SOPs, and regulatory guidanceDemonstrates solid interpersonal skillsExhibits strong self-motivation, detail-oriented and able to work and plan independently as well as in a team environmentGood written and verbal communication skillsAbility to deliver on commitmentsCommitment to performing professionally consistent with our clients and Precision PrinciplesPrecision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics.

Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease. It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature.

Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process. Apply Now