OR · On-site
The Senior Clinical Research Associate is responsible for the overall operational execution of ... Partner with other research and development groups at Natera to achieve deliverables * Perform ...
OR · On-site
The Senior Clinical Research Associate is responsible for the overall operational execution of ... Partner with other research and development groups at Natera to achieve deliverables * Perform ...
San Carlos, CA · On-site
$74K - $93K/yr
Join Natera's R&D Scientific Operations as a Research Associate 2 on the Sample Processing team ... clinical diagnostic assays. Every sample represents a real person, and you will ensure accuracy ...
San Carlos, CA · On-site
$74K - $93K/yr
Join Natera's R&D Scientific Operations as a Research Associate 2 on the Sample Processing team ... clinical diagnostic assays. Every sample represents a real person, and you will ensure accuracy ...
Dayton, OH · On-site
$110K - $130K/yr
Become experts on all Natera Oncology products and processes to maximize effectiveness in the field ... Associate's degree with minimum of 4 years of relevant experience * Medical assistant, clinical ...
Dayton, OH · On-site
$110K - $130K/yr
Become experts on all Natera Oncology products and processes to maximize effectiveness in the field ... Associate's degree with minimum of 4 years of relevant experience * Medical assistant, clinical ...
Dayton, OH · On-site
$110K - $130K/yr
Become experts on all Natera Oncology products and processes to maximize effectiveness in the field ... Associate's degree with minimum of 4 years of relevant experience * Medical assistant, clinical ...
Dayton, OH · On-site
$110K - $130K/yr
Become experts on all Natera Oncology products and processes to maximize effectiveness in the field ... Associate's degree with minimum of 4 years of relevant experience * Medical assistant, clinical ...
Become experts on all Natera Oncology products and processes to maximize effectiveness in the field ... Associate's degree with minimum of 4 years of relevant experience * Medical assistant, clinical ...
Become experts on all Natera Oncology products and processes to maximize effectiveness in the field ... Associate's degree with minimum of 4 years of relevant experience * Medical assistant, clinical ...
Memphis, TN · On-site
$65K - $114K/yr
The Clinical Research Associate - RN also provides patient care, education, and management. Position has a dotted line reporting relationship to the Nursing Executive/CNO. Coordinates with supervisor ...
Memphis, TN · On-site
$65K - $114K/yr
The Clinical Research Associate - RN also provides patient care, education, and management. Position has a dotted line reporting relationship to the Nursing Executive/CNO. Coordinates with supervisor ...
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative ...
Quick apply
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative ...
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative ...
Quick apply
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative ...
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative ...
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative ...
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative ...
Quick apply
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative ...
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative ...
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative ...
Los Angeles, CA · On-site
$25 - $36.86/hr
The Clinical Research Associate II works independently but in close collaboration with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, other supervising staff to ...
Los Angeles, CA · On-site
$25 - $36.86/hr
The Clinical Research Associate II works independently but in close collaboration with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, other supervising staff to ...
The Clinical Research Associate II works independently but in close collaboration with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, other supervising staff to ...
The Clinical Research Associate II works independently but in close collaboration with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, other supervising staff to ...
ICON plc is seeking an experienced Senior Clinical Research Associate (Senior CRA) or Clinical Research Associate (CRA) to join our dynamic, collaborative team. In this role, you will be a key ...
ICON plc is seeking an experienced Senior Clinical Research Associate (Senior CRA) or Clinical Research Associate (CRA) to join our dynamic, collaborative team. In this role, you will be a key ...
This TI Clinical Research Associate will be known internally as a Float Clinical Research Associate (Float CRA). It is a collaborative role supporting clinical research programs of the Knight Cancer ...
This TI Clinical Research Associate will be known internally as a Float Clinical Research Associate (Float CRA). It is a collaborative role supporting clinical research programs of the Knight Cancer ...
$18.99 - $28.51/hr
Position Details Additional Information Posting Category Research - Non Academic Working Title Clinical Research Associate l Job Title clinical research Associate L1 Salary Grade RA14H Appointment ...
$18.99 - $28.51/hr
Position Details Additional Information Posting Category Research - Non Academic Working Title Clinical Research Associate l Job Title clinical research Associate L1 Salary Grade RA14H Appointment ...
Los Angeles, CA · On-site
$25 - $36.86/hr
The Clinical Research Associate II works independently but in close collaboration with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, other supervising staff to ...
Los Angeles, CA · On-site
$25 - $36.86/hr
The Clinical Research Associate II works independently but in close collaboration with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, other supervising staff to ...
Omaha, NE · On-site
$18.99 - $28.51/hr
Position Details Additional Information Posting Category Research - Non Academic Working Title Clinical Research Associate l Job Title clinical research Associate L1 Salary Grade RA14H Appointment ...
Omaha, NE · On-site
$18.99 - $28.51/hr
Position Details Additional Information Posting Category Research - Non Academic Working Title Clinical Research Associate l Job Title clinical research Associate L1 Salary Grade RA14H Appointment ...
The Senior Clinical Research Associate is responsible for overseeing the execution of clinical trials at Investigative Sites. The Clinical Research Associate acts as a liaison between the study ...
The Senior Clinical Research Associate is responsible for overseeing the execution of clinical trials at Investigative Sites. The Clinical Research Associate acts as a liaison between the study ...
Memphis, TN · On-site
Together with a clinical ethicist and 2.5 clinical research associate FTE, the team provides clinical and research ethics consultation services, produces original scholarship in bioethics, and ...
Memphis, TN · On-site
Together with a clinical ethicist and 2.5 clinical research associate FTE, the team provides clinical and research ethics consultation services, produces original scholarship in bioethics, and ...
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7.6
Based on 37 frontline employees who took The Breakroom Quiz
60th of 120 rated laboratories
POSITION SUMMARY:
The Senior Clinical Research Associate is responsible for the overall operational execution of clinical studies on one or more clinical projects/programs; from study concept through study completion. This position will perform required job duties with guidance from Clinical Trial Managers to ensure that trial timelines, costs, and quality metrics are met, and the study is conducted in compliance with the study protocol, SOPs, and applicable regulatory requirements helps design and execute clinical research activities.
PRIMARY RESPONSIBILITIES:
Provide high level logistical support for clinical study operations, including study start up, study supplies, site qualification, site initiation, site management, study monitoring, and close out for clinical research studies and collaborations
Develop study-related documents with minimal Clinical Trial Manager guidance including: protocol, informed consent forms, training materials, protocol amendments, monitoring plans, synopses, and ethics committee submissions, as required
Manage small to medium size study contracting, budget, invoicing and payment process for all clinical trial vendors including investigative sites with minimal oversight
Support the Clinical Data Management team in the design and content of case report forms, completion guidelines, including support and testing of an EDC
Manage the preparation, handling, filing, and archiving of clinical documentation and reports according to SOPs and study requirements
Overseeing clinical trial supplies related to biospecimen collection, processing, shipment, and storage as, well as maintenance of associated tracking information
Train CROs, vendors, investigators, and study coordinators on study requirements and provide guidance on site issues
Monitor and track clinical trial progress, provide status updates to stakeholders
Develop new study monitoring plans, and monitor studies following study monitoring plans to identify protocol deviations or data discrepancies
Perform study activities including consent participants for research studies, ethics board submissions, participant data and sample tracking using in-house and CRO databases, for studies where Natera functions as a Clinical Research Site.
Update Clinical Department SOPs with guidance from CTM and/or Director
Partner with other research and development groups at Natera to achieve deliverables
Perform other duties as assigned
This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper and electronic) in order to perform the job.
Employee must provide records of current training or complete training relating to HIPAA/PHI privacy, Human Subjects Protection, and GCP.
Must maintain a current status on Natera training requirements including General Policies, Procedure Compliance, and security training
Employee must pass post offer criminal background check
QUALIFICATIONS:
BA/BS degree in life sciences, related field, or equivalent
Minimum of 4 years of experience working on clinical studies in the academic, biopharma, diagnostics, or medical device fields
KNOWLEDGE, SKILLS AND ABILITIES:
Experience with clinical EDC systems,
Familiarity with the organization and structure of the Trial Master File (TMF)
Familiarity with bio sample management, sample processing, and biobanking best practices
Competency in SOPs, ICH-GCP, FDA Regulations
Proficiency in MS Word, Excel and PowerPoint
Demonstrated ability to work independently and lead projects
Demonstrated analytical skills and ability to identify complicated problems and propose solutions
Strong interpersonal skills and communication skills (both written and oral)
Excellent writing skills
Detail oriented, with solid organization and time management skills