Senior Clinical Research Associate
Employment Information
Report this job
Job expired or something wrong with this job?
Job Description
Senior Clinical Research Associate at Natera responsible for overall execution of clinical studies. Collaborating with Clinical Trial Managers to meet trial timelines, costs, and regulatory compliance.
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.
Requirements:
- 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.
Benefits:
- Comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents.
- Free testing for employees and their immediate families in addition to fertility care benefits.
- Pregnancy and baby bonding leave.
- 401k benefits.
- Commuter benefits.
- Generous employee referral program!
Similar Jobs
Senior Clinical Research Associate – EU, Medical Devices
Senior Clinical Research Associate managing CRO oversight and clinical monitoring for pivotal trials. Focused on compliance, quality, and patient safety in innovative cardiac care at Anteris Technologies.
Clinical Research Associate II – Sponsor Dedicated
Clinical Research Associate II role in monitoring clinical research studies for Syneos Health. Conducting compliance checks and collaborating with teams to ensure smooth study execution.
Clinical Research Associate
Clinical Research Associate conducting site qualification, monitoring, and management duties for clinical trials. Ensuring regulatory compliance and site performance across the drug development process.
Senior Clinical Research Associate I
Senior Clinical Research Associate responsible for site management in oncology studies for Parexel. Collaborating with experts and utilizing advanced technology in a supportive environment.
Research Analyst – VoC
Research Analyst focusing on customer experience research and VoC initiatives at an e-commerce company. Collaborating with cross-functional teams to drive insights and recommendations based on player feedback.
Study Start-Up Clinical Research Associate, Sponsor Dedicated
Study Start-Up Clinical Research Associate at IQVIA managing site selections and start-up activities for clinical trials. Collaborating with teams to ensure on-time delivery of study commitments while maintaining quality standards.
Freelance Clinical Research Associate
Freelance Clinical Research Associate managing clinical studies with pediatric monitoring experience. Join Rho in Bulgaria and ensure compliance with SOPs and regulatory requirements.
Clinical Research Associate, Sponsor Dedicated
Clinical Research Associate managing study sites and monitoring compliance under GCP guidelines. Collaborating with project teams to enhance predictability and execute studies efficiently.
Education Policy and Applied Research Analyst
Education Policy and Applied Research Analyst supporting LSAC’s mission through research and data insights. Collaborating with stakeholders to produce high-quality educational research and reports.
In-House Clinical Research Associate
In-House Clinical Research Associate at Rho managing clinical trial monitoring and data management activities. Collaborating with CRAs and project managers to ensure compliance with study protocols and regulations.
Senior Clinical Research Associate
Senior Clinical Research Associate ensuring integrity and quality in clinical trials for a growing CRO. Joining a collaborative team dedicated to addressing significant healthcare challenges.
Clinical Research Associate
Clinical Research Associate monitoring clinical trials for drug development at Praxis Precision Medicines. Ensuring compliance and conducting site management to improve patients' lives.
Bilingual Senior Clinical Research Associate
Manage clinical site monitoring services for multinational projects as Lead CRA. Responsible for design, oversight, and collaboration with stakeholders.
Desk Research Specialist
Senior Desk Research Specialist for Ek Kutumb conducting rigorous research into values and beliefs shaping communities across India. Anchoring secondary research and promoting informed policy design.
Qualitative Research Associate
Qualitative Research Associate at Ek Kutumb conducting research on social values and community beliefs. Engaging with diverse communities across India to gather qualitative insights on social change.
Research Associate, Survey – Education
Research Associate managing survey administration and project logistics for Hanover Research's growing enterprise. Collaborating with project managers and external vendors to streamline survey processes.
In-House Clinical Research Associate
In-House Clinical Research Associate at ICON plc supporting the execution and management of clinical trials. Contributing to innovative treatments and therapies.
Senior Research Consultant – On Call
On-call Senior Research Consultant providing expertise on workforce development and research. Collaborating with clients to lead and support strategic consulting projects in social issue areas.
Senior Clinical Research Associate, Site Manager
Senior Clinical Research Associate overseeing clinical trials in compliance with regulations. Collaborating with study centres and ensuring quality while managing study documentation and data validation.
Research Associate, SEPP
Research Associate contributing to projects in special education and policy evaluation at WestEd. Collaborating on research proposals and coordinating project management activities.