Senior Clinical Research Associate
OR · On-site +1
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 +1
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 +1
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
$108K - $135K/yr
We are looking for a highly motivated Senior Research Associate with a strong focus on process ... Work with Clinical Laboratory and Quality Assurance to ensure that developed methods meet Natera ...
New
San Carlos, CA · On-site
$108K - $135K/yr
We are looking for a highly motivated Senior Research Associate with a strong focus on process ... Work with Clinical Laboratory and Quality Assurance to ensure that developed methods meet Natera ...
New
We are looking for a highly motivated Senior Research Associate with a strong focus on process ... Work with Clinical Laboratory and Quality Assurance to ensure that developed methods meet Natera ...
New
We are looking for a highly motivated Senior Research Associate with a strong focus on process ... Work with Clinical Laboratory and Quality Assurance to ensure that developed methods meet Natera ...
New
Austin, TX · On-site
... clinical assays are developed and launched for our patients. The ideal candidate will be an ... The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory ...
Austin, TX · On-site
... clinical assays are developed and launched for our patients. The ideal candidate will be an ... The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory ...
OR · On-site +1
Join Natera's Clinical Innovation & Therapeutics team as a Medical Science Liaison (MSL) in ... Support and coordinate clinical trial and research initiatives at academic institutions and study ...
OR · On-site +1
Join Natera's Clinical Innovation & Therapeutics team as a Medical Science Liaison (MSL) in ... Support and coordinate clinical trial and research initiatives at academic institutions and study ...
San Carlos, CA · On-site
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
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 ...
$141K - $176K/yr
... Natera training requirements. QUALIFICATIONS: * Bachelor's degree in life sciences, other relevant discipline, or equivalent required. Advanced degree preferred. * 5-10 years of clinical research ...
$141K - $176K/yr
... Natera training requirements. QUALIFICATIONS: * Bachelor's degree in life sciences, other relevant discipline, or equivalent required. Advanced degree preferred. * 5-10 years of clinical research ...
Austin, TX · On-site
POSITION SUMMARY: The IVD Product Development Research Associate 1 will assist with various ... Must maintain a current status on Natera training requirements. QUALIFICATIONS: * BS/BA in a ...
New
Austin, TX · On-site
POSITION SUMMARY: The IVD Product Development Research Associate 1 will assist with various ... Must maintain a current status on Natera training requirements. QUALIFICATIONS: * BS/BA in a ...
New
OR · On-site +1
Collaborate with R&D, biostatistics, clinical operations, and HEOR on protocol development ... Ability to rapidly master Natera's core technologies and competitive landscape, communicating ...
OR · On-site +1
Collaborate with R&D, biostatistics, clinical operations, and HEOR on protocol development ... Ability to rapidly master Natera's core technologies and competitive landscape, communicating ...
Collaborate with R&D, biostatistics, clinical operations, and HEOR on protocol development ... Ability to rapidly master Natera's core technologies and competitive landscape, communicating ...
Collaborate with R&D, biostatistics, clinical operations, and HEOR on protocol development ... Ability to rapidly master Natera's core technologies and competitive landscape, communicating ...
OR · On-site +1
... Natera training requirements. QUALIFICATIONS: * Bachelor's degree in life sciences, other relevant discipline, or equivalent required. Advanced degree preferred. * 5-10 years of clinical research ...
OR · On-site +1
... Natera training requirements. QUALIFICATIONS: * Bachelor's degree in life sciences, other relevant discipline, or equivalent required. Advanced degree preferred. * 5-10 years of clinical research ...
Asbury Park, NJ · On-site
$110K - $130K/yr
The Associate Clinical Oncology Specialist (ACOS) is responsible for contributing to account sales ... Become experts on all Natera Oncology products and processes to maximize effectiveness in the field.
New
Asbury Park, NJ · On-site
$110K - $130K/yr
The Associate Clinical Oncology Specialist (ACOS) is responsible for contributing to account sales ... Become experts on all Natera Oncology products and processes to maximize effectiveness in the field.
New
Fairmont, WV · On-site
$110K - $130K/yr
Associate Clinical Oncology Specialist Bridgeport, WV; Fairmont, WV This territory encompasses most ... Become experts on all Natera Oncology products and processes to maximize effectiveness in the field.
Fairmont, WV · On-site
$110K - $130K/yr
Associate Clinical Oncology Specialist Bridgeport, WV; Fairmont, WV This territory encompasses most ... Become experts on all Natera Oncology products and processes to maximize effectiveness in the field.
Toledo, OH · On-site
$80K - $100K/yr
The Associate Clinical Oncology Specialist (ACOS) is responsible for contributing to account sales ... Become experts on all Natera Oncology products and processes to maximize effectiveness in the field.
Toledo, OH · On-site
$80K - $100K/yr
The Associate Clinical Oncology Specialist (ACOS) is responsible for contributing to account sales ... Become experts on all Natera Oncology products and processes to maximize effectiveness in the field.
Bridgeport, WV · On-site
$110K - $130K/yr
The Associate Clinical Oncology Specialist (ACOS) is responsible for contributing to account sales ... Become experts on all Natera Oncology products and processes to maximize effectiveness in the field.
Bridgeport, WV · On-site
$110K - $130K/yr
The Associate Clinical Oncology Specialist (ACOS) is responsible for contributing to account sales ... Become experts on all Natera Oncology products and processes to maximize effectiveness in the field.
Bridgeport, WV · On-site
$110K - $130K/yr
The Associate Clinical Oncology Specialist (ACOS) is responsible for contributing to account sales ... Become experts on all Natera Oncology products and processes to maximize effectiveness in the field.
Bridgeport, WV · On-site
$110K - $130K/yr
The Associate Clinical Oncology Specialist (ACOS) is responsible for contributing to account sales ... Become experts on all Natera Oncology products and processes to maximize effectiveness in the field.
El Paso, TX · On-site
$110K - $130K/yr
Associate Clinical Oncology Specialist This role covers the entire state of New Mexico and El Paso ... Become experts on all Natera Oncology products and processes to maximize effectiveness in the field.
El Paso, TX · On-site
$110K - $130K/yr
Associate Clinical Oncology Specialist This role covers the entire state of New Mexico and El Paso ... Become experts on all Natera Oncology products and processes to maximize effectiveness in the field.
Syracuse, NY · On-site
$110K - $130K/yr
The Associate Clinical Oncology Specialist (ACOS) is responsible for contributing to account sales ... Become experts on all Natera Oncology products and processes to maximize effectiveness in the field.
Syracuse, NY · On-site
$110K - $130K/yr
The Associate Clinical Oncology Specialist (ACOS) is responsible for contributing to account sales ... Become experts on all Natera Oncology products and processes to maximize effectiveness in the field.
Atlanta, GA · On-site
$110K - $130K/yr
Northeast Atlanta The Associate Clinical Oncology Specialist (ACOS) is responsible for contributing ... Become experts on all Natera Oncology products and processes to maximize effectiveness in the field.
Atlanta, GA · On-site
$110K - $130K/yr
Northeast Atlanta The Associate Clinical Oncology Specialist (ACOS) is responsible for contributing ... Become experts on all Natera Oncology products and processes to maximize effectiveness in the field.
Syracuse, NY · On-site
$110K - $130K/yr
The Associate Clinical Oncology Specialist (ACOS) is responsible for contributing to account sales ... Become experts on all Natera Oncology products and processes to maximize effectiveness in the field.
Syracuse, NY · On-site
$110K - $130K/yr
The Associate Clinical Oncology Specialist (ACOS) is responsible for contributing to account sales ... Become experts on all Natera Oncology products and processes to maximize effectiveness in the field.
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7.7
Based on 38 frontline employees who took The Breakroom Quiz
57th 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
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Biotechnology research and development
1,001 - 5,000 Employees
Austin, TX, US