Senior Clinical Research Associate

As a Clinical Research Associate you will be responsible for monitoring clinical trials and ensuring investigators are conducting research within the requirements of the clinical protocol and ICH-GCP. You will be involved in all stages of clinical trials, including the identification of an investigational site and setting up, initiating, monitoring and closing down a trial. You will work closely with the project team in order to ensure compliance with appropriate regulations and guidelines throughout the trial and will conduct data analysis to ensure this meets the required clinical standards. You will ensure the rights and safety of human subjects involved in a clinical study are protected at all times.Position Accountabilities/Responsibilities:Participate in the investigator recruitment process, performing initial qualification visits of potential investigators and evaluating the capability of the site to successfully manage and conduct the clinical study, both clinically and technicallyWork with the study start up group to coordinate activities with the site in preparation for the initiation of studiesManage regulatory authority applications and approvals, obtaining regulatory documentation for successful implementation, monitoring and evaluation of clinical trialsSet up trial sites, ensuring that each center has the necessary trial materialsWork with the study start up group and site staff to obtain regulatory (IRB/IEC) approval of study specific documentsEnsure study documentation is maintained in the Investigator Study File and where necessary ensure relevant documents are transferred or copied to the (electronic) Trial Master FilePerform study initiation activities, reviewing with the site personnel, the protocol, regulatory issues and study proceduresProvide training on completion of the eCRF; monitoring activities and study close out activitiesTrain site staff on the EDC system and verify site computer systemMonitor trials throughout their duration, conducting periodic site file audits to ensure compliance with GCP and the company’s standard operating proceduresEnsure adherence to Good Clinical Practice, investigator integrity and compliance with all study procedures through on site monitoring visitsPerform validation of study data against source documentation as required by the sponsor and prepare monitoring reports and letters as necessaryDocument accountability, stability and storage conditions of clinical trial materials as required by the sponsorPerform investigational product inventory and ensure return of unused materials to designated location/verify destruction as requiredReview the quality and integrity of clinical data through in house review of electronic CRF data and on-site source verificationWork with sites to resolve any data queries as requiredAssist with and attend investigator meetings for assigned studiesDeveloping and reviewing protocols, eCRFs, study manuals and other related documents as requested by the Clinical Trial LeadCoordinate with the ethics committee in order to ensure the rights, safety and well being of all trial subjects including provision of updates according to local requirementsAct as the primary contact between Catalyst and the investigator, coordinating all correspondence and ensuring timely transmission of clinical data with the study site and technical reporting as necessaryAssist with final data review and query resolution through to database lockPerform study close out visits and archive study documentation and correspondenceAct as a mentor for new clinical research associatesSupervisory Requirements/Responsibilities:Strategic thinkingAbility to Act decisivelyMotivating performanceWorking collaborativelyCoaching and developing othersPosition Qualifications and Requirements:Education

: Degree or equivalent qualification in life sciences or allied discipline with proven experience in the field of monitoring ideally early phase Oncology, Rare Diseases, Cell and Gene Therapies .Experience

:

2+ years

of monitoring experience with strong focus on oncology.Required Certifications

: N/ARequired Skills

:Sound knowledge of clinical research process and medical terminologyGood understanding of electronic data capture, including basic data processing functionsGood understanding of current ICH-GCP (R2) guidelines applicable to the conduct of clinical researchWillingness and ability to travel domestically (and occasionally internationally) as requiredProven ability to lead and influence at study sites and in a fast paced and collaborative environmentExcellent verbal and written communication and interpersonal, negotiation and conflict resolution skillsStrong organisational skills with an ability to multi task and work independentlyStrong technical skills using PowerPoint, Excel and Word

Working Conditions:

​Sedentary work that primarily involves sitting/standing.​ Employee may be office or home based with regular business travel.