trial disclosure / clinical trial submissions associate

trial disclosure / clinical trial submissions associate.

north chicago , illinois (remote)

posted today

job details

summary

$38 – $42.48 per hour

contract

bachelor degree

category life, physical, and social science occupations

reference46827

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 youre 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: $38.00 – 42.48 per hour

work hours: 7 to 3

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 metrics

Monitor CTIS notifications received, due dates and trends

Identifies 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.

qualifications:

Bachelors degree required, preferably in a health or biological science field

1-3 yrs experience in clinical trial registries, regulatory agency transparency or drug development with a clinical research, quality or regulatory background, preferably in a pharma industry environment

Comfortable learning new systems

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

Works well in a global, team environment

Available for early hours to support EU colleagues (i.e. start time as early as 7a Central)

skills: GCP (Good Clinical Practice), ICH Regulations

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 candidates 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).