Clinical research associate jobs in Oakland, CACreate job alerts

Job Summary: Provides mental health assessment, diagnosis, treatment and crisis intervention services for adult and/or child members who present themselves from psychiatric evaluation with a broad range of mental health needs. Collaborates with treating physician, psychiatric and allied health ...

As a Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.Contribute to the identification of new sites for clinical trials; analyse capability and support CRMA and CSM in making recommendation

Job Summary: Under supervision of a Licensed Clinical Social Worker, Licensed Marriage Family Therapist or a Licensed Professional Clinical Counselor, provides mental health assessment and triage, diagnosis, treatment and crisis intervention services for adult and/or child members who present t...

Job Summary: Provides mental health assessment, diagnosis, treatment and crisis intervention services for adult and/or child members who present themselves from psychiatric evaluation with a broad range of mental health needs. Collaborates with treating physician, psychiatric and allied health ...

As a Senior Clinical Research Associate, you will support the Clinical Development Team in ensuring the execution of assigned trials according to the study timelines and company goals and in compliance with ICH GCP, country regulations, and SOPs. This role provides the opportunity to expand one's...

Research Associate on the non-clinical development team, the selected candidate will be responsible for manufacturing oncolytic viral vectors and performing experiments to support translational research to advance these therapies from discovery to the clinic. Research Associate, Non-Clinical Deve...

Research Associate on the non-clinical development team, the selected candidate will be responsible for manufacturing oncolytic viral vectors and performing experiments to support translational research to advance these therapies from discovery to the clinic. Research Associate, Non-Clinical Deve...

As a Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Contribute to the identification of new sites for clinical trials; analyse capability and support CRMA and CSM in making recommendatio

The Senior Clinical Research Associate (Sr CRA) will independently manage all clinical aspects of a small to medium-sized clinical study or, with supervision, assume significant management responsibilities on a large-scale study. Clinical Research Associate- Contract. Overall management of select...

The Senior Clinical Research Associate (Sr CRA) will independently manage all clinical aspects of a small to medium-sized clinical study or, with supervision, assume significant management responsibilities on a large-scale study. Clinical Research Associate- Contract. Overall management of select...

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Contribute to the identification of new sites for clinical trials; analyse capability and support CRMA and CSM in making recommendat

The Senior Clinical Research Associate (Sr CRA) will independently manage all clinical aspects of a small to medium-sized clinical study or, with supervision, assume significant management responsibilities on a large-scale study. Clinical Research Associate- Contract. Overall management of select...

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Ability to work effectively with investigators and other research personnel, maintaining a professional demeanor. Contribute to the

Seeking for an experienced Clinical Research Associate who will be responsible for providing Clinical Research support for a biotech company. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to clinical research functions. Assi...

As a Clinical Research Associate you will be joining the worlds largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Contribute to the identification of new sites for clinical trials; analyse capability and support CRMA and CSM in making recommendation ...

The Senior Clinical Research Associate (Sr CRA) will independently manage all clinical aspects of a small to medium-sized clinical study or, with supervision, assume significant management responsibilities on a large-scale study. Clinical Research Associate- Contract. Overall management of select...

The Senior Clinical Research Associate (Sr CRA) will independently manage all clinical aspects of a small to medium-sized clinical study or, with supervision, assume significant management responsibilities on a large-scale study. Clinical Research Associate- Contract. Overall management of select...

The CRA will ensure quality, accuracy, and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials according to the Code of Federal Regulations, ICH GCP, and ISO14155. Assist and conduct clinical monitoring and site management activities, ensuring compliance to ...

The Senior Clinical Research Associate (Sr CRA) will independently manage all clinical aspects of a small to medium-sized clinical study or, with supervision, assume significant management responsibilities on a large-scale study. Clinical Research Associate- Contract. Overall management of select...

Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial management systems; data analysis; and data reporting and interpretation. The CRA II will assist in the clinical execution and managem...

The Clinical Research Coordinator (CRC) will be responsible for providing clinical and administrative support to the Principal Investigator (PI) for a variety of research studies conducted in the SFVAHCS Cardiac Catheterization Laboratory (CCL). The CRC will be responsible for the coordination of...

Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial management systems; data analysis; and data reporting and interpretation. Perform review of clinical data listings for completeness an...

Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial management systems; data analysis; and data reporting and interpretation. The CRA II will assist in the clinical execution and managem...

Seeking for an experienced Clinical Research Associate who will be responsible for providing Clinical Research support for a biotech company. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to clinical research functions. Unde...

Reporting to the Senior Clinical Trial Manager, the Senior Clinical Research Associate will participate in planning and assisting in overseeing the conduct of clinical trials in accordance with Company policies and procedures and applicable regulations. Sponsor, CRO, or site experience (Senior Cl...

This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Assess the clinical research site's patient recruitment and retention success and offering sugges...

Job Title : Project Manager – Veeva Vault.Founded in 1998 and headquartered in Farmington Hills, MI, Kyyba has a global presence delivering high-quality resources and top-notch recruiting services, enabling businesses to effectively respond to organizatio.

Responsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to clinical research functions. Initiate studies performing initiation site visits, arrange for shipm...

Telecommuting permitted on hybrid basis.Salary: $130,000 - $160,000/ year.

Responsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to clinical research functions. Under the direction of supervisor or designee, this position will ser...

It has direct responsibility for implementing a diverse portfolio of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored) local investigator-initiated clinical trials and/or programmatic clinical research activities such as a ...

Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial management systems; data analysis; and data reporting and interpretation. Manage clinical monitoring activities and overall site manag...

The Clinical Research Coordinator will perform independently at the fully operational journey level of the series to execute manage and coordinate research protocols as directed by the Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical re...

Hospitals on Incredible Health are actively hiring and accepting applications for Cardiac Cath Lab Technicians in the Oakland area.Shift(s) available: day shift, mid shift, and night shift - Job types available: full-time, part-time, and per diem - Employer features: competitive compensation, ret...

At ngrok we believe that doing networking the right way should also be the easy way.Over the last 10 years weve given developers and engineers simple interfaces for getting traffic into their apps and APIs without forcing them to deal with legacy proxies external load balancers or VPNs and were n...

Perform impact analysis of new regulations from a quantitative perspective and identify any financial risks associated with the regulations.

The HDFCCC integrates the work of researchers and clinicians dedicated to four fundamental pursuits: laboratory research into the causes of cancer progression; clinical research to translate new knowledge into viable treatments; compassionate state-of-the-art patient care; and population research...

Research Scientists/Engineers (all levels). Foundation Model / Fundamental AI Research institute. Come join one of the only research institutions globally with resources to compete with top AI companies =>.

Hospitals on Incredible Health are actively hiring and accepting applications for Cardiac Cath Lab Technicians in the Oakland area.The following information aims to provide potential candidates with a better understanding of the requirements for this role.Shift(s) available: day shift, mid shift,...

Ready to be the heartbeat of medical research? Join our client as an In Vivo Research Associate and assist in turning innovative science into life-changing care! Proclinical is seeking an In Vivo Research Specialist to provide essential support for in vivo studies involving mice. Part-Time In Viv...

This is a journey-level License Project Manager job that is responsible for managing one or more moderately large and complex regulatory projects (“license projects”) related to the Federal Energy Regulatory Commission (FERC) licenses and associated lands for the Company’s extensive hydroelect

Experience with SAP and Power BI is preferred.Create dashboards and report inventory.Create a catalog of data fields with definitions.Identify reports and dashboards using various fields.Provide organizational support.Create usage reports and governance on the accessibility of multiple reports.Cr...

Experience with SAP and Power BI is preferred.Create dashboards and report inventory.Create a catalog of data fields with definitions.Identify reports and dashboards using various fields.Provide organizational support.Create usage reports and governance on the accessibility of multiple reports.Cr...

Location: San Francisco (Remote Eligible).Salary: $200K–$240K base + Equity.We’re hiring a Staff Product Analyst for a hyper-growth, Series E AI company valued at $3B+.This is an opportunity to play a key role in shaping product strategy and growth by leveraging data to drive decisions, optimize

Coordinating, monitoring, and supervising all aspects of clinical studies from start-up to closeout, to ensure proper execution of assigned clinical research trials and to ensure that study protocols are me. As a Clinical Research Coordinator, you will lead the study team and be responsible for t...

Coordinating, monitoring, and supervising all aspects of clinical studies from start-up to closeout, to ensure proper execution of assigned clinical research trials and to ensure that study protocols are me. As a Clinical Research Coordinator, you will lead the study team and be responsible for t...

AlliedTravelCareers is working with Atlas MedStaff to find a qualified Medical Lab Technician in San Leandro, California, 94577!.Atlas Medstaff is currently seeking candidates in the Med Lab Tech (Med Lab Tech) profession for a 13 week contract in the San Leandro, California area.Atlas Medstaff i...

Develop and QC TFLs for protocols/reports/manuscripts from RWE research conducted to assess the value of our client's therapies using RWD (e. Work with RWE researchers to generate code lists for new measures in RWD. MA, MSc, MPH) in Biostatistics, Epidemiology or related discipline, such as Outco...