Clinical Research Coordinator

2 weeks ago

Manchester, United Kingdom MastarRec Full time

Job DescriptionWe are seeking detail-oriented Clinical Research Coordinator (CRC) to oversee and manage clinical trial activities ensuring strict adherence to GCP guidelines regulatory requirements and study protocols. You will play a critical role in coordinating all aspects of clinical research from participant recruitment to data management and compliance monitoring to support the delivery of groundbreaking medical advancements.This is an exciting opportunity to work at the intersection. Of healthcare innovation patient care and research excellence in a collaborative fast-paced environment.Job ResponsibilitiesCoordinate and manage the day-to-day operations of clinical studiesRecruit screen and consent eligible study participants in accordance with IRB-approved protocolsMaintain accurate and up-to-date source documentation and electronic data capture (EDC) systemsMonitor patient safety schedule study visits and ensure protocol adherenceLiaise with principal investigators sponsors and ethics committeesPrepare regulatory documentation site initiation and close-out reportsTrack study progress and submit timely updates to stakeholdersEnsure quality assurance and compliance with ICH-GCP MHRA and institutional regulationsRequirementsRequired SkillsIn-depth knowledge of GCP clinical research regulations and ethical standardsExperience with clinical data collection source documentation and informed consent processesProficiency with electronic data capture systems (e.g. REDCap Medidata or similar)Strong organizational and time management skillsExcellent communication and interpersonal abilitiesDetail-oriented and able to handle multiple trials simultaneouslyDesired SkillsBachelors degree in Life Sciences Nursing or Health SciencesACRP or SOCRA certificationPrevious experience in oncology cardiology or rare disease clinical trialsFamiliarity with clinical trial software platforms and regulatory submissionsBenefitsJob BenefitsCompetitive salary with annual performance bonusesTraining and career development in clinical operations and trial managementPrivate health insurance and pension planSupportive work environment with flexible working optionsWork with a cross-disciplinary team of clinical and research expertsRequired Skills: Required Skills Strong knowledge of PCR ELISA Western blotting Data recording and lab documentation skills BSc or MSc in Molecular Biology/Biotech Desired Skills CRISPR or RNA-based tech exposure GLP/GMP environment familiarity Key Skills CSS,Cloud Computing,Health Education,Actuary,Building Electrician Employment Type : Full Time Experience: years Vacancy: 1 Yearly Salary Salary: 38000 - 52000

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