Clinical Project Associate

Integrated Resources Inc.Foster City

On-site Full-time

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Experience Level

Entry Level

Qualifications

Qualifications for the Clinical Project Associate position include:Bachelor's degree in a relevant field (e.g., Life Sciences, Nursing, or related disciplines). Strong organizational skills with the ability to manage multiple tasks efficiently. Excellent communication skills, both written and verbal. Detail-oriented with a proactive approach to problem-solving. Ability to work effectively in a team environment.

About the job

We are seeking a dedicated and detail-oriented Clinical Project Associate to join our team. In this role, you will support the management and execution of clinical trials, ensuring compliance with regulatory requirements and internal protocols. Your contributions will be vital in facilitating the progress of clinical studies from initiation through completion.

If you are passionate about clinical research and eager to contribute to innovative medical solutions, we encourage you to apply!

About Integrated Resources Inc.

Integrated Resources Inc. is a leading provider of innovative solutions in the healthcare sector, dedicated to improving patient outcomes through advanced clinical research. Our team is committed to excellence and integrity, striving to make a meaningful impact in the medical field.

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Clinical Data Associate II

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Full-time|On-site|Foster City

Join our team as a Clinical Data Associate II, where you will play a crucial role in supporting clinical trials and ensuring the integrity of clinical data. You will be responsible for data management processes, including data collection, validation, and reporting. Your attention to detail and analytical skills will be essential in maintaining high data qual…

Mar 6, 2017

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Clinical Data Associate

Integrated Resources Inc.

Full-time|On-site|Foster City

We are seeking a detail-oriented and highly organized Clinical Data Associate to join our dynamic team. In this role, you will be responsible for managing clinical trial data, ensuring accuracy and compliance with regulatory requirements. You will work closely with clinical research teams to support the successful execution of clinical studies.

May 26, 2017

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Clinical Data Associate III

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Full-time|On-site|Foster City

Join our dynamic team as a Clinical Data Associate III, where you will play a pivotal role in managing and analyzing clinical data to support our clinical trials. We are looking for a skilled professional who is detail-oriented and has a strong understanding of data management processes in clinical research.

Aug 22, 2017

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Clinical Project Associate II

Integrated Resources Inc.

Full-time|On-site|Foster City

We are seeking a dedicated and detail-oriented Clinical Project Associate II to join our dynamic team. In this role, you will actively support clinical project management activities, ensuring the successful execution of clinical trials and adherence to regulatory standards.

Apr 17, 2017

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Clinical Records Associate - II

Integrated Resources, Inc.

Full-time|On-site|Foster City

Job Title: Clinical Records Associate - IILocation: Foster City, CADuration: 12 MonthsJob Description: Fulfill all responsibilities of a Clinical Records Assistant and exhibit proven expertise in relevant domains.Possess a strong understanding of Good Clinical Practice (GCP), International Council for Harmonisation (ICH), and Good Laboratory Practice (GLP) regulations regarding the management and preservation of clinical trial and preclinical study documentation.Maintain a comprehensive knowledge of clinical, biometrics, and preclinical documentation.Contribute to the ongoing security and maintenance of the Trial Master File (TMF) Room.Support the formulation and execution of procedures for the establishment, security, and upkeep of Trial Master Files for both clinical and preclinical studies.Assist in the creation of Standard Operating Procedures (SOPs) for Trial Master Files.Help train both Client and contract personnel on TMF SOPs.Engage in the management of vendor relationships, including offsite document storage.Establish and maintain study-specific file structures for clinical, biometrics, and preclinical documents, ensuring accurate filing.Keep record filing current and precise.Conduct inventory reviews for incoming CRO clinical study files; manage the reception, indexing, and filing of preclinical study records; oversee offsite document archiving; take part in periodic TMF utilization assessments; file incoming documents and retrieve documentation from the TMF Room upon request.Ensure the appropriate documentation is completed to track archival of files.May provide support during regulatory agency inspections related to TMF and internal GCP inspections.Assist in developing electronic tracking and filing systems.

Sep 6, 2017

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Clinical Data Manager

Integrated Resources Inc.

Full-time|On-site|Foster City

Join Integrated Resources Inc. as a Clinical Data Manager and play a pivotal role in advancing our clinical research initiatives. In this dynamic position, you will oversee clinical data management processes, ensuring data integrity and compliance with regulatory standards.Your responsibilities will include managing data collection, validation, and analysis, and collaborating with cross-functional teams to drive project success. This is an exciting opportunity for individuals passionate about data in the healthcare sector.

Jul 20, 2017

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Clinical Research Coordinator / Clinical Project Associate

Integrated Resources Inc.

Full-time|On-site|Foster City

We are seeking a dedicated and detail-oriented Clinical Research Coordinator / Clinical Project Associate to join our dynamic team. In this role, you will play a key part in managing clinical trials, ensuring adherence to regulatory standards, and facilitating communication between stakeholders. Your expertise will help to advance innovative research that has the potential to improve patient outcomes.

Jul 18, 2017

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Clinical Research Associate

Integrated Resources Inc.

Full-time|On-site|Foster City

We are seeking a dedicated and detail-oriented Clinical Research Associate to join our dynamic team. In this role, you will play a vital part in overseeing clinical trials and ensuring compliance with regulatory standards. Your expertise will help in the management of study protocols, patient recruitment, and data collection, contributing to the advancement of medical research.

Feb 21, 2017

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Clinical Trials Management Associate – II

Integrated Resources Inc.

Full-time|On-site|Foster City

Join Integrated Resources Inc. as a Clinical Trials Management Associate – II and play a pivotal role in advancing medical research. In this dynamic position, you will collaborate with cross-functional teams to manage clinical trial operations, ensuring compliance with regulatory standards and timelines. Your ability to thrive in a fast-paced environment will be key as you contribute to the successful execution of clinical trials.

Feb 14, 2017

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Clinical Data Manager

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Full-time|On-site|Foster City

We are seeking a detail-oriented Clinical Data Manager to join our dynamic team in Foster City, California. In this role, you will be responsible for overseeing the clinical data management lifecycle, ensuring data integrity, and supporting clinical trial operations. You will collaborate closely with cross-functional teams to facilitate the effective collection, analysis, and reporting of clinical data.

Aug 21, 2017

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Clinical Trials Management Associate II

Integrated Resources, Inc.

Full-time|On-site|Foster City

Join our dedicated team as a Clinical Trials Management Associate II, where you will play a vital role in overseeing clinical trials from initiation to completion. You will collaborate with cross-functional teams to ensure compliance with regulatory standards and protocols, while contributing to the advancement of innovative therapies. Your expertise will help drive projects forward in a dynamic and supportive environment.

Apr 18, 2017

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Clinical Project Associate

Integrated Resources, Inc.

Full-time|On-site|Foster City

Join our dynamic team at Integrated Resources, Inc. as a Clinical Project Associate. In this role, you will be crucial in supporting clinical research projects from inception to completion. Your responsibilities will include coordinating project activities, managing timelines, and ensuring compliance with regulatory requirements.

Aug 22, 2017

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Clinical Project Associate

Integrated Resources Inc.

Full-time|On-site|Foster City

Jan 7, 2017

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Clinical Data Associate Opportunity at Integrated Resources Inc. | Foster City

Integrated Resources Inc.

Full-time|On-site|Foster City

We are seeking a detail-oriented and motivated Clinical Data Associate to join our dynamic team at Integrated Resources Inc. In this role, you will play a crucial part in managing and analyzing clinical data, ensuring its accuracy and integrity throughout the research process.

Aug 8, 2017

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Clinical Project Associate

Integrated Resources, Inc.

Full-time|On-site|Foster City

Join Integrated Resources, Inc. as a Clinical Project Associate where you will play a vital role in supporting clinical research projects. This position is perfect for individuals eager to advance their career in clinical trials and project management. You will collaborate closely with cross-functional teams to ensure that projects are executed efficiently and in compliance with regulatory standards.

Mar 30, 2017

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Clinical Trials Management Associate

Integrated Resources, Inc.

Full-time|On-site|Foster City

Join Integrated Resources, Inc. as a Clinical Trials Management Associate, where you will play a vital role in overseeing clinical trial operations. You will collaborate with cross-functional teams to ensure the effective execution of clinical studies while adhering to regulatory standards.

May 24, 2017

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Clinical Records Associate

Integrated Resources, Inc.

Contract|On-site|Foster City

* Develop a foundational understanding of GCP, ICH, and GLP regulations related to the organization and preservation of clinical trial documentation and preclinical study records. * Contribute to the ongoing security and upkeep of the Trial Master File (TMF) Room. * Engage in offsite storage activities. * Construct and manage study-specific file structures for clinical, biometrics, and preclinical documents, ensuring proper filing of all documents. * Maintain accurate and up-to-date record filing. * Conduct inventory reviews for incoming CRO clinical study files; receive, index, and file preclinical study records; oversee offsite archiving of documents; participate in regular reviews of file room utilization; file incoming documents and retrieve documentation from the TMF Room upon request. * May assist in preparing for TMF-related inspections by regulatory agencies and internal GCP readiness assessments. * Support the creation of electronic tracking and filing systems.

Sep 12, 2017

Apply

Clinical Project Associate

Integrated Resources, Inc.

Full-time|On-site|Foster City

Join Integrated Resources, Inc. as a Clinical Project Associate, where you will play a crucial role in supporting our clinical operations and project management teams. In this dynamic position, you will assist in the planning, execution, and monitoring of clinical trials while ensuring compliance with regulatory standards and timelines. Your responsibilities will include coordinating project timelines, managing documentation, and facilitating communication among various stakeholders. This role is ideal for someone passionate about clinical research and eager to contribute to innovative healthcare solutions.

Jul 3, 2017

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Clinical Project Associate

Integrated Resources Inc.

Full-time|On-site|Foster City

As a Clinical Project Associate at Integrated Resources Inc., you will play a crucial role in the management and coordination of clinical trials. You will assist in the planning, execution, and monitoring of clinical projects to ensure they are conducted in compliance with regulatory standards. Your responsibilities will include collaborating with cross-functional teams, maintaining project documentation, and supporting project timelines.

Mar 13, 2017

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Clinical Project Associate

Integrated Resources, Inc.

Full-time|On-site|Foster City

Join Integrated Resources, Inc. as a Clinical Project Associate, a pivotal role where you will contribute to the successful execution of clinical trials. In this position, you will support project management activities, coordinate meetings, and ensure compliance with regulatory requirements. Your attention to detail and strong communication skills will be essential in facilitating collaboration among cross-functional teams.

Feb 2, 2017

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