benefits associate salaries in chicago, illinois

job summary: Join a leading biopharmaceutical team at their fully remote North Chicago, IL site as a Trial Disclosure Associate. This is a fantastic opportunity for professionals with a background in clinical research, regulatory affairs, or trial transparency to play a key role in supporting global clinical trial disclosures. You'll work closely with cross-functional teams to ensure timely and accurate submissions through the Clinical Trial Information System (CTIS), helping drive transparency and regulatory compliance on a global scale. Ideal candidates bring strong attention to detail, comfort learning new systems, and at least 1-3 years of experience in clinical trial registries or drug development. You'll thrive in a structured yet fast-paced environment where collaboration, clear communication, and the ability to juggle shifting priorities are highly valued. This is an excellent chance to build your expertise in trial disclosure operations while contributing to high-impact projects that support critical therapeutic programs.   location: Telecommute job type: Contract salary: $35 - 42 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Support clinical trial applications submitted via Clinical Trial Information System (CTIS), uploading documents, QCing documents uploaded to ensure accurate categorization.Track CTIS application details to compile metricsMonitor CTIS notifications received, due dates and trendsIdentifies system conflicts and resolves or elevates them to management to ensure resolution.Exhibits a moderate level of technical competencies and requires a low level of counsel and guidance.Completes activities to assist in ensuring timely disclosure of accurate, consistent, aligned and complete information globally.Communicates deliverables, process and timelines effectively across functional areas and within department to accomplish project objectives.Continually trains/is compliant with all current SOPs & work instructions.Cross trains with other Trial Disclosure staff.  qualifications: Required Skills: Bachelor's degree (preferably in a health or biological science field)1-3 years of experience in clinical trial registries, regulatory transparency, or drug developmentBackground in clinical research, regulatory, or quality within the pharmaceutical industryStrong attention to detail (ability to identify and correct errors in spelling, grammar, consistency, and accuracy)Comfortable learning and navigating new systemsAbility to manage shifting daily priorities and meet deadlinesProficient in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook)Effective written and verbal communication skillsWorks well in a global team environmentAvailable to work early hours to support EU colleagues (as early as 7 AM CST) Preferred Skills: Direct experience with CTIS or clinical trial disclosure platformsFamiliarity with global regulatory requirements for trial disclosureExperience working in a large pharmaceutical company or global organizationAbility to analyze trends and compile metricsExposure to SOP-driven environments and cross-functional collaboration #LI-AM1   skills: Trial Data Management, Trial Disclosure Equal 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 HRsupport@randstadusa.com. Pay 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. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

job summary: This remote opportunity is ideal for a highly experienced pharmacovigilance professional ready to apply their in-depth knowledge of ICSR case processing. As a Subject Matter Expert, you will be the first line of decision-making for case processing issues, ensuring the highest standards of quality and global compliance. The role offers the chance to collaborate with internal and external parties, provide critical input on training materials, and troubleshoot a wide variety of complex problems. This position is perfect for a technical expert who thrives on improving processes and safeguarding compliance for a major pharmaceutical company.   location: Telecommute job type: Contract salary: $50 - 62 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Communicates with internal and external parties on case contents, and to reply to related queriesMakes first line decisions on case processing matters for prioritization, FU significance, seriousness, labeling, coding queries, etcPerforms or initiates case corrections, as neededPerforms SME services for ICSR processing queries by the vendorSupports late case investigations by the regional PV Case Management team.Provides Subject Matter Expertise (medical/technical.) for the creation of training materials in collaboration with the PV Training team.Facilitates finalized training sessions (PV Processes and systems) for vendors and PV Process staff in collaboration with PV Training team.   qualifications: Education & Qualifications Required: MS degree in life sciences or equivalent5+ years relevant experience with ICSR case processing (PV case processing) and expertise within PharmacovigilanceIn-depth knowledge and understanding of PV Process regulatory requirements and ICSR processing procedures globally and in Americas regionA technical expert within the organization, with extensive knowledge within their chosen specialty and developing knowledge of related disciplines.Has the ability to recommend enhancements to internal policies, processes and procedures based on new requirements, legislation, etc.Provides solutions to a wide variety of problems of greater complexity that require the regular use of creativity and ingenuity, while safeguarding Astellas' compliance.Ensures case processing and case quality are maintained at highest standards at all timesStrong interpersonal skills and multi-cultural /intercultural awareness; able to develop effective relationships through collaboration.Good communication skills in English (written and spoken) Preferred: RN  skills: Pharmacovigilance Equal 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 HRsupport@randstadusa.com. Pay 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. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Ready to take advantage of growth opportunities at some of the top companies in your area? Reliable production associates who are comfortable working in high-speed environments and motivated by overtime pay should be sure to apply. Read on for more information. The application process itself only takes a moment, and if you're qualified, we'll get back to you promptly.location: Schaumburg, ILwork hours: 09:00 PM - 06:00 AMqualifications:up to 50 lbs. (heavy lifting)skills:Inspect quality and defects of productsAssemble products according to specificationsdress code:Shirts or t-shirts must have sleeves and be without any holes or rips. Pants without any holes or rips. No profane or suggestive texts and images. Closed toe and non slip footwear only. No jewelry. Equal 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 HRsupport@randstadusa.com.Pay 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.