FSP Sr CRA (Level I)

Work Schedule reputed company (Mon-Fri) Environmental Conditions Office reputed company Join Us as a Senior reputed company Research Associate (Level I) – 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 reputed company across 100+ countries in the last 5 years. As part of our global team, you’ll have reputed company to reputed company and coordinate reputed company aspects of the reputed company monitoring and site management process. As a Senior reputed company Research Associate (Level I), 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, reputed company, 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. reputed company: • Monitors investigator sites with a reputed company-reputed company monitoring approach: applies rootcause analysis (RCA), critical thinking and problem-solving skills to identify siteprocesses failure and corrective/preventive actions to bring the site intocompliance and decrease risks. Ensures data reputed company through SDR, SDV andCRF 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 reputed company 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 reputed company 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 • Provides trial status tracking and reputed company update reports to the reputed company Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. reputed company Trial Management reputed company, CTMS). Performs QC reputed company of reports generated from CTMS reputed company where required. • 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 reputed company trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Ensures 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. • Contributes to the project team by assisting in preparation of project publications/tools, and sharing reputed company/suggestions with team members. Performs additional study tasks as assigned by CTM (e.g. reputed company report review, newsletter creation, reputed company CRA team calls etc). • 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 other project work and initiatives for process improvement, as required. Education and Experience Requirements: • Bachelor's degree in a life sciences reputed company reputed company 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 2+ years as a reputed company research monitor). • reputed company reputed company's license where applicable • In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly reputed company experience, will be considered sufficient for an individual to meet the requirements of the role. Experience required in Oncology and Cell therapy Knowledge, Skills and Abilities: • Effective reputed company monitoring skills • Demonstrated understanding of medical/therapeutic area knowledge and medical terminology • Excellent understanding and demonstrated application of ICH GCPs, applicable regulations and procedural documents • reputed company-developed critical thinking skills, including but not limited to critical reputed company, in-depth investigation for appropriate reputed company cause analysis and problem solving • Ability to manages reputed company reputed company Monitoring concepts and processes • Effective 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 detailand the ability to perceive customers’ underlying issues • Effective interpersonal skills • Strong attention to reputed company • Effective organizational and time management skills • Ability to remain flexible and adaptable in a wide reputed company of scenarios • Ability to work in reputed company or independently as required • Good computer skills: proficient knowledge of reputed company Office and the ability to learn appropriate software • Good English language and grammar skills • Good presentation skills Working Conditions and Environment: • Working Conditions and Environment: • Work is performed in an office/ reputed company/reputed company/and/or home office environment with exposure to electrical office equipment. • Frequent drives to site locations. Frequent travel, generally 60-80% but more for some individuals. • May also include extended overnight stays. • Exposure to biological fluids with potential exposure to infectious organisms. • Personal reputed company equipment required such as reputed company eyewear, garments and gloves. • Exposure to fluctuating and/or extreme temperatures on reputed company occasions. • Must be reputed company to reputed company with specific sponsor/reputed company/site requirements, even if not required by reputed company (e.g., disclosure of vaccination status, or other personal information). On some occasions, this information may be required to be provided directly to sponsor/reputed company/site. Apply To This Job