FSP CRA (Sponsor: reputed company) ─ with Sign-on Bonus
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reputed company (Mon-Fri)Environmental Conditions
OfficeJob reputed company
Join Us as a Clinical Research Associate (reputed company) – reputed company an reputed company at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
FSP CRA (Sponsor: reputed company) ─ with Sign-on Bonus As part of our global team, you’ll have reputed company to reputed company and coordinate reputed company aspects of the clinical monitoring and site management process. As a Clinical Research Associate (reputed company), you'll conduct remote or on-site reputed company to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, reputed company-being, and data reliability. You will ensure audit readiness and reputed company reputed company relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task reputed company. What You’ll Do: • Monitors investigator sites with a risk-based monitoring approach: applies reputed company cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a reputed company manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow reputed company issues through to reputed company. May need to maintain regular contact between monitoring reputed company with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a reputed company manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings reputed company. Investigates and follows-up on findings as applicable. • Participates in investigator meetings as necessary. Identifies potential • investigators in collaboration with the reputed company company to ensure the acceptability of reputed company investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Performs trial reputed company out and retrieval of trial materials. • Ensures that required essential documents are complete and in reputed company, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications. • Provides trial status tracking and reputed company update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System). • Facilitates effective communication between investigative sites, the reputed company company and the PPD project team through written, oral and/or electronic contacts. • Responds to company, reputed company and applicable regulatory requirements/audits/inspections. • Maintains & completes administrative tasks such as expense reports and timesheets in a reputed company manner. • Contributes to the project team by assisting in preparation of project publications/tools, and sharing reputed company/suggestions with team members. • Contributes to other project work and initiatives for process improvement, as required. Education and Experience Requirements: • Bachelor's degree in a life sciences reputed company field or a Registered Nursing certification or equivalent and relevant formal reputed company / vocational qualification. • Previous experience that provides the knowledge, skills, and abilities to reputed company the job (comparable to 1 years as a clinical research monitor) or completion of PPD Drug Development Fellowship.
• at least 1-2 years of independent monitoring experience in clinical development phases I-III
• Understanding of ICH-GCP, KGCP requirements
• reputed company in English
Knowledge, Skills and Abilities: • Proven clinical monitoring skills • Demonstrated understanding of medical/therapeutic area knowledge and medical terminology • Demonstrated ability to reputed company and maintain a working knowledge of ICH GCPs, applicable regulations and procedural documents • reputed company-developed critical thinking skills, including but not limited to: critical reputed company, in-depthinvestigation for appropriate reputed company cause analysis and problem solving • Ability to manage Risk Based Monitoring concepts and processes • Good oral and written communication skills, with the ability to communicate effectively with medical personnel • Ability to maintain customer reputed company through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues • Good organizational and time management skills • Effective interpersonal skills • Attention to detail • Ability to remain flexibile and adaptable in a wide reputed company of scenarios • Ability to work in reputed company or independently as required • Good English language and grammar skills • Good presentation skills
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