at Randstad US in north chicago, Illinois, United States
Job Description
trial disclosure associate ii.
+ north chicago , illinois (remote)
+ posted june 28, 2024
job details
summary
+ $40 – $48.95 per hour
+ contract
+ bachelor degree
+ category life, physical, and social science occupations
+ reference48387
job details
job summary:
As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you’re looking to stand out in your field and lead the way to innovative therapies, this position is for you!
location: North Chicago, Illinois
job type: Contract
salary: $40.00 – 48.95 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
+ Responsibilities will be focused on supporting EU CTR applications and documentation. Familiarity with clinical study and site start up documentation is preferred.
+ Responsibilities will vary based upon business need. May support global study registrations, writing scientific study results, protocol/result lay summaries, or anonymizing clinical documents for public disclosure by regulatory agencies.
+ 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.
+ Coordinates the review, approval, and other appropriate functions.
+ Identifies conflicts and resolves or elevates them to management to ensure resolution.
+ Holds team members accountable to agreed-upon project dates. Negotiates with functional areas on project outcomes and deliverables to meet conflicting demands (time, deliverables, etc.).
+ Exhibits a moderate level of technical competencies and requires a low level of counsel and guidance.
+ Continually trains/is compliant with all current SOPs & work instructions.
qualifications:
+ Bachelor’s degree required, preferably in a health or biological science field
+ 2-4 yrs experience in clinical trial registries, regulatory agency transparency or drug development with a clinical research, quality or regulatory background, preferably in a pharma environment
+ Project management experience preferred
+ 2 years of writing experience preferred
+ Attention to detail. Find and correct errors in spelling, punctuation, grammar, consistency, clarity and accuracy.
+ Ability to shift daily priorities, meet deadlines, ask questions
+ Proficient with major Microsoft suite programs and other pharma systems
+ Works well in a global, team environment
skills: MS-WORD, CTMS (Clinical Trial Management Systems)
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 health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).
This posting is open for thirty (30) days.
