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1 week ago Be among the first 25 applicantsGet AI-powered advice on this job and more exclusive features.Job SummaryAs a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on oncology, cardiology, and bone health. With a strong legacy of scientific excellence and a mission to improve patient outcomes worldwide, they offer a dynamic environment where your contributions will drive real change. If you're seeking a rewarding career that makes a difference, let us help you take the next step!Job SummaryAs a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on oncology, cardiology, and bone health. With a strong legacy of scientific excellence and a mission to improve patient outcomes worldwide, they offer a dynamic environment where your contributions will drive real change. If you're seeking a rewarding career that makes a difference, let us help you take the next step!Key SkillsNursing degree neededDrug SafetyPharmacovigilanceMedical review/ Safety Reviewlocation: Telecommutejob type: Contractsalary: $60.00 - 69.09 per hourwork hours: 9 to 5education: BachelorsResponsibilitiesResponsibilitiesExecute the medical review of ICSRs (narratives, coding, expectedness, causality and seriousness) to ensure quality reports. Produce medically accurate ICSRs reportsAct as MSRT product lead as assignedExecute ICSR case escalation as appropriateExecute appropriate case follow up per SOPsSupport medical coding conventions, and systematic process improvements for ICSR medical reviewMaintain list of expected terms in the auto label toolSupport Quality Assurance of ICSR medical reviewParticipate in Safety Assessment Team (SAT) (if applicable)Conduct reportability assessment for medical device associated events and /or product complaint associated events, and review for potential product problemsProvide input on teams for interdepartmental and cross-functional initiatives (if applicable)Perform other duties related to the position as necessary as defined in SOPs or as requested by his/her supervisorInspection ReadinessUndertake activities delegated by the QPPV as detailed in the PV System Master File and maintain a state of inspection readinessBe representative and point of contact for Health Authority Inspection and Internal Process Audits within the remit of role and responsibilityQualificationsRequired:Clinical Nursing qualification + 1 year drug safety experience.Nursing Degree + 3 years relevant work experience.Medical review of ICSRs (narratives, coding, expectedness, causality, seriousness).Quality Assurance of ICSR medical review.Clinical knowledge of therapeutic area patient populations and drug class.skills: Quality Assurance, ICSR (Individual Case Study Report), QC ReviewEqual Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).This posting is open for thirty (30) days.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance.Qualified applicants in the unincorporated areas of Los Angeles County with criminal histories will be considered for employment in accordance with the Los Angeles County's Fair Chance Ordinance for Employers.We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.u00006475229Seniority levelSeniority levelNot ApplicableEmployment typeEmployment typeContractJob functionJob functionResearch, Analyst, and Information TechnologyIndustriesPharmaceutical ManufacturingReferrals increase your chances of interviewing at Randstad Life Sciences US by 2xGet notified about new Medical Researcher jobs in Thousand Oaks, CA.Clinical Research Principal Investigator MD/DOSenior Medical Science Liaison (Sr. MSL) / Principal Medical Science Liaison (Principal MSL) Oncology - Northern CA and Los AngelesNorthridge, CA $32,244.00-$201,276.00 1 year agoPhysician - Medical Oncology - Simi Valley, CASenior Registered Nurse - VCMC Nursing EducationVentura, CA $118,668.43-$141,888.74 1 month agoThousand Oaks, CA $30.00-$32.00 6 days agoAssociate Scientist (Animal handling, oncology)Clinical Fellow: Speech Language PathologistClinical Fellow: Speech-Language PathologistNurse Practitioner or Physician Assistant OncologyPhysical Therapist - Ortho/Oncology - Up to $20k bonusThousand Oaks, CA $130,000.00-$196,000.00 4 days agoWe're unlocking community knowledge in a new way. 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