17 Clinical Study Coordinator Jobs in Austin, TX
Diasorin is Hiring a Clinical Study Coordinator Near Austin, TX
- Impactful Work: When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world.
- Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry.
Job Scope
The Clinical Study Coordinatorplays an integral role in supporting the conduct of analytical and clinical studies involving Luminex in vitro diagnostic devices, planning and execution of in-house clinical studies, and qualification and monitoring of external clinical sites in accordance with Clinical Affairs timeline requirements. The role also involves activities related to the logistical requirements for the execution of clinical studies in accordance with applicable global regulations and standards (e.g. 21 CFR Part 812, CLSI, ICH) that demonstrate the performance and utility of in vitro diagnostic products.
Key Duties and Responsibilities
- Day-to-day "hands on" work associated with in-house clinical studies.
- Collection and analysis of experimental data generated in-house and externally.
- Assist with site qualification processes and support monitoring of external clinical sites in accordance with study protocols and applicable regulations and standards (eg. 21 CFR Part 812, GLP, CLSI, ICH)
- Develop study tools and forms (eg. Enrollment logs, Data Record Forms, Case Report Forms etc.)
- Coordinate execution of site contracts and site budget preparation
- Coordinate and track clinical supplies shipped and used at clinical sites.
- Collaborates with sample bank to acquire and dispense clinical specimens for use at external clinical sites.
- Maintenance of study documentation and data history files
- Maintain working knowledge of current protocols and internal SOPs.
- Interact with other internal Luminex departments and external service providers, if required (eg. Sequencing facilities, CROs)
- Additional Product Development & Clinical tasks, as need arises.
- Other duties as assigned.
Education, Experience, and Qualifications
- Bachelor's Degree technical subject plus at least 3 years' work experience. required or
- Bachelor's Degree in chemistry, biology, molecular biology or a related subject, with additional post-graduate diploma or 1 year work experience preferred but not required; preferred or
- Master's Degree technical subject plus at least 2 years' work experience; preferred
- 1 Years Previous work experience with clinical trials, analytical or method validation studies preferred. preferred
- Excellent communication, organizational and time management skills
- Proficiency with Microsoft Office software
What we offer
Receive a competitive salary and benefits package as you grow your career at DiaSorin. Join our team and discover how your work can impact the lives of people all over the world.
Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability.In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and Canada and to complete the required employment eligibility verification document form upon hire.Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities. If you are a US or Canada candidate and require assistance or accommodation during the application process, please contact the North America Talent Acquisition Team at hrtalent@diasorin.com or 1-800-328-1482 to request an accommodation.The above job description is intended to describe the general content, identify the essential functions, and set forth the requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or requirements.Diasorin reserves the right to modify or amend this job posting as needed to comply with local laws and regulations.Please note that offers of employment at Diasorin may be contingent upon successful completion of a pre-employment background check and drug screen, subject to applicable laws and regulations.This position is not eligible for partnership with a third-party search firm vendor without expressed, written consent from the Diasorin Human Resources Department. We are an equal opportunity employer that values diversity at all levels. All individuals, regardless of personal characteristics, are encouraged to apply.This contractor and subcontractor shall abide by the requirements of 41 CFR 60-1.4(a), 41 CFR 60-300.5(a) and 41 CFR 60-741.5(a). These regulations prohibit discrimination against qualified individuals based on their status as protected veterans or individuals with disabilities, and prohibit discrimination against all individuals based on their race, color, religion, sex, sexual orientation, gender identity or national origin. Moreover, these regulations require that covered prime contractors and subcontractors take affirmative action to employ and advance in employment individuals without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.
DiaSorin Inc and DiaSorin Molecular LLC are Affirmative Action and Equal Opportunity Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
Job Summary
Full Time
$56k-74k (estimate)
03/27/2024
05/26/2024
cn.diasorin.com
<25
The job skills required for Clinical Study Coordinator include Clinical Trial, Patient Care, Microsoft Office, Innovation, Time Management, Background Check, etc. Having related job skills and expertise will give you an advantage when applying to be a Clinical Study Coordinator. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Clinical Study Coordinator. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Clinical Study Coordinator positions, which can be used as a reference in future career path planning. As a Clinical Study Coordinator, it can be promoted into senior positions as a Clinical Research Manager that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Study Coordinator. You can explore the career advancement for a Clinical Study Coordinator below and select your interested title to get hiring information.
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