This job posting may have expired!
Use our `search` to find similar offers.
Similar jobs

Clinical Operations Associate II

Charles River Laboratories International Inc (CRL)

Memphis, TN, US, 38118

Clinical Operations Associate II Req ID #:  161834 Location: 

Memphis, TN, US, 38118 Memphis, TN, US, 38118 For 70 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

IMPORTANT:   In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process.  Please make sure work history and education are added correctly.    Job Summary OBJECTIVE

This position will provide assistance in the management of clinical operations in support of investigational studies contracted at Cognate facilities.

 

 

ESSENTIAL DUTIES/RESPONSBILITIES

•Assist in coordination of clinical supplies, receipt of patient tissues for processing, and investigational product shipment

•Assist in coordination of the timely completion of clinical supply activities through close interactions with Materials Management, Manufacturing, Operations and Quality Assurance Departments, while working collaboratively with multiple clients.

•Assist in coordination of clinical patient events within Cognate BioServices

•Serve as a designated contact for assigned clinical projects

•Field calls and questions pertaining to assigned study specific tasks

•Actively participate in planned weekly meetings, as assigned

•Assist in providing regular status updates, as designated by Department Head/Manager

•Participate in development of appropriate action plans to prevent or correct deficiencies

•Provide assistance in development/enforcement of departmental SOPs

•Ability to effectively apply GXP and applicable regulatory guidelines, as required

•Participate in the writing of SOPs and other documentation, as required

  Job Qualifications  

•Bachelor's degree in science or a related life sciences field. Must have a minimum three (3) years of experience in clinical trial studies or related programs.

•Good understanding of clinical trial study design and its relevance

•Strong knowledge of GXP (GMP, GLP, GTP)

•Experience in activities related to quality, logistics, etc. for cell-based therapeutic products

•Working knowledge of cell processing methods

•Excellent planning and organizational skills and proven ability to multitask and manage time and work

•Proven interpersonal, facilitation, customer relations and negotiation skills

•Ability to utilize initiative and work independently

•Possess good communication skills, both verbal and written

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV. 

Vaccine Mandate

Charles River is a U.S. Federal Contractor.  As a result, we must follow the Presidential Executive Order to mandate vaccinations, and ensure our employees are fully vaccinated against COVID-19.  Our main priority is the wellbeing, health, and safety of our people. We require proof of vaccination from all employees. 

Anyone with requests for disability-related and/or religious exemptions should contact Talent Acquisition (crrecruitment_US@crl.com) so that information can be provided about the accommodation process at Charles River.

 

About Cognate BioServices

Cognate BioServices, Inc., a Charles River Company, is the premier commercial-ready CDMO for cell and gene therapy needs. We are a dynamic, results-driven organization focused on providing the broadest range of expertise across the various cell types and technologies used in the commercialization of cell & gene therapies for regenerative medicine, cellular immunotherapy, and advanced cell therapy companies, organizations, and institutions.

We offer a unique combination of standard and custom services to companies across all points of clinical and commercial development. Our development and manufacturing services are focused on clients seeking rapid development of products from clinical studies into commercial manufacturing, with a unique capacity to handle all aspects of scale-up and commercial readiness.

Cognate leverages the combined know-how and expertise of its business, scientific, and technical teams to successfully develop and manufacture autologous and allogenic products across multiple cell-based technology platforms from start to finish, for you and your patients.

For more information, visit www.cognatebioservices.com 

Equal Employment Opportunity

Charles River Laboratories 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, veteran or disability status.

 

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

 

For more information, please visit www.criver.com.

Nearest Major Market: Memphis

Job Segment: Operations Manager, Telecom, Telecommunications, Supply, Operations, Technology

Job posted: 2022-04-01

3