Postdoctoral Research Associate jobs in Camano Island, WA

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Senior Clinical Research Associate (CONTRACTOR / IC)
  • 1281 Parexel International (South Africa)(PTY) Limited
  • Lynnwood, WA PART_TIME
  • When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. The Clinical Research Associate is the clinical sites’ direct point of contact and accountable for managing site quality and delivery from site identification through close-out. The aim of this role is to build the relationship with the site, to be the sole position accountable for the site performance, including driving the site successfully to initiation, the development of a robust patient recruitment strategy, setting up a system, assessing compliance with regulations and the site’s capability to comply with the study needs and recruitment expectations, and problem solving to address and resolve site issues. This may include various tasks and roles within the CRA framework, contingent upon project phase and country demands, and complexity of the study. The Clinical Research Associate will oversee the conduct of the trial at designated sites, ensuring the rights and well-being of human subjects are protected, evaluating the quality and integrity of the reported data, evaluating the site efficacy of staff training and requiring retraining where necessary, developing strategy regarding patient recruitment, evaluating and building the relationship with the clinical site, using problem-solving to promote positive working relationships with the site and staff, and ensuring the conduct of the trial is in compliance with the currently approved protocol/amendment(s), with GCP and with the applicable regulatory requirement(s). Where available an “initiation Clinical Research Associate“ (iCRA) specializing in Pre SIV activities will be assigned & accountable for managing and driving the strategy for the Pre SIV / startup tasks of the study. The iCRA) also support protocol amendments if applicable. Key Accountabilities: Start-up (from site identification through pre-initiation): Act as Parexel’s direct point of contact with assigned sites, accountable for quality and delivery during the start-up phase. Build relationships with investigators and site staff. Conduct, drive and manage country specific feasibility and/or site pre-qualification and qualification activities, which may include: -Preparation, negotiation, and facilitation of execution of Confidentiality Agreements (CDA), Clinical Site Agreements (CSAs) and any amendments. -Conduct remote Qualification Visits (QVs). Generate visit/contact reports, using judgment to identify site issues and problem solving to direct resolution. Develop strategy to configure, distribute, and collect, and review and approve, high quality country specific and/or site specific documents or essential regulatory documents (SRP) and any updated or amended regulatory documentation. Customize, review, and negotiate as needed, country/site specific Informed Consent Forms (ICF), translations (within parameters of country/regulatory/client requirements), and customize and negotiate any amendments. Prepare and submit IRB/IEC and MoH/RA (if applicable) application(s), resolving conflicts, determining appropriate follow up until receipt of final approval. Submit all pertinent documentation to the trial master file as per project plans/sponsor/company policy. Forecast, develop, manage, and revise plans and strategies for: -IRB/IEC and MoH / RA submission/approval, -Site activation, -Patient recruitment & retention. Update and maintain appropriate Clinical Trial Management systems (CTMS) in a timely manner. Promptly identify, use judgment and knowledge to address and resolve or escalate, any site question and/or issue, including but not limited to: potential issues or risks with site activation timelines, issues with patient recruitment strategy, deficiencies in training, data quality or integrity, study non-compliance, etc. Facilitate and support allocated sites with access to relevant study systems and ensure they are compliant with all project specific training requirements prior to study start. Actively participate in Investigator and other external or internal meetings, audits & regulatory inspections Work in a self-driven capacity, with limited need for oversight. Proactively keep manager informed about work progress and any issues. Maintenance (from initiation through close out): Act as Parexel’s direct contact with assigned sites, assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites, and perform problem-solving to address and resolve site issues. Build relationships with investigators and site staff. Facilitate and support site with access to relevant study systems and ensure sites are compliant with project specific training requirements. Evaluate if on-site staff assignment is still accurate and determine and implement corrective actions & follow-up, if necessary / relevant. Address and resolve issues at sites, including the need for additional training, potential deficiencies in documentation, and communication. Address/evaluate/resolve issues pending from the previous visit, if any. Follow-up on and respond to appropriate site related questions. Apply working knowledge and judgment to identify and evaluate potential data quality and data integrity issues. Determine and implement appropriate follow-up action. Actively participate in Investigator and other external or internal meetings and audits & regulatory inspections as required. Collect, review, and approve (if applicable) updated/amended site documentation, including regulatory documents as applicable. Evaluate site recruitment plan in collaboration with the site staff on an ongoing basis and provide strategy for improvements. Perform on-site visits; this includes Qualification and Initiation visits; apply judgment and knowledge to independently resolve site issues, questions and concerns. Conduct remote visits/contacts as requested/needed. Generate visit/contact report. Evaluate overall compliance and performance of sites and site staff: provide recommendations regarding site-specific actions and use judgment and experience to assess the ability and motivation of site staff. Assess & manage test article/study supply including supply, accountability and destruction/return status. Review & follow-up site payment status. Follow-up on CRF data entry, query status, and SAEs. Conduct on-site study-specific training (if applicable). Perform site facilities assessments Recognize impact of study non-compliance/issues/delays/changes on study timelines and communicate study issues that require immediate action, with proposed strategy for resolution Overall Accountabilities from Site Identification to Close out: Ensure timely and accurate completion of project goals and update of applicable trial management systems. Work with team members to meet project goals, provide strategy for efficient project planning and goal completion, and encourage the support of team members where required. Update all appropriate Clinical Trial Management Systems (CTMS) on an ongoing basis, including performing regular reviews of site level data in clinical systems (e.g. CTMS, EDC, IVRS, and SIS) and ensure timely and high quality data entry compliance from sites, manage and submit all relevant documents to the Trial Master File (TMF), ensuring first time quality, and distribute study documents to site including configuration of Investigator Site Files if applicable and on-going maintenance for completeness and quality. Ensure that assigned sites are audit and inspection ready Monitor and maintain compliance with ICH-GCP and applicable international and local regulations. Delegate administrative and other tasks to Administrative Support Team as needed and where appropriate. Guide Administrative Support Team members, review work, and provide feedback to manager regarding performance. Show commitment and perform consistent high quality work. Maintain a positive, results-orientated work environment, building partnerships and collaborative relationships, communicating with team(s) in an open, balanced, objective manner, modeling the high performance culture values. Maintain a working knowledge of and ensure compliance with applicable ICH-GCP Guidelines, international and local regulations, Parexel SOPs, other Parexel / Sponsor training requirements and study specific procedures, plans and training. Ensure basic understanding of project scope, milestones, budgets, and strive for high quality, timely, and efficient delivery. Provide input and feedback for Performance Development Conversation(s). Proactively keep manager informed about work progress and any issues. Develop expertise to become a subject matter expert. Work in a self-driven capacity, with limited need for oversight. Complete additional tasks in a timely manner (e.g. timesheets, expenses, metrics, etc.) Skills: Strong problem solving skills Able to take initiative and work independently, and to proactively seek guidance when necessary. Excellent presentation skills. Client focused approach to work. Ability to interact professionally within a client organization. Flexible attitude with respect to work assignments and new learning. Ability to prioritize multiple tasks, and achieve project timelines; utilizing strong analytical skills to make decision autonomously due to the unpredictable nature of the issues that arise. Strong ability to make appropriate decisions in ambiguous situations. Willingness to work in a matrix environment and to value the importance of teamwork. Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products such as Excel and Word. Excellent interpersonal, verbal, and written communication skills. Sense of urgency in completing assigned tasks and ability to assist others to meet study/country deliverables. Excellent time management in order to meet study needs, team objectives, and department goals. Proven ability to work across cultures. Shows commitment to and performs consistently high quality work. Ability to successfully work in a (‘virtual’) team environment. Consulting Skills. Able to accommodate travel time requirements, according to tasks allocation/phase of the study assigned. Act as a mentor and role model for other team members. Effectively enlist the support of team members in meeting goals. Attention to detail. Holds a driver’s license where required. Knowledge and Experience: Substantial Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology Education: Educated to degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification or other equivalent experience Headquartered near Boston, Massachusetts and in Durham, North Carolina, Parexel has over 16,000 employees, with offices that support clients in over 100 countries around the world. We provide the most comprehensive drug development capabilities of any CRO worldwide. Our global regulatory expertise, Phase I-IV clinical research services, and advanced commercialization services all work together to move you through the development journey more smoothly and cost-effectively from beginning to end.
  • 14 Days Ago
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Data entry clerk
  • Maxion Research
  • Oak Harbor, WA FULL_TIME
  • Remote Work From Home Data Entry Clerk for Entry Level Position Work at home position for job seekers from virtually any work background who are interested in part-time, side gigs, micro jobs, work fr...
  • 19 Days Ago
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Data entry specialist
  • Maxion Research
  • Lynnwood, WA FULL_TIME
  • Remote Work From Home Data Entry Clerk for Entry Level Position Work at home position for job seekers from virtually any work background who are interested in part-time, side gigs, micro jobs, work fr...
  • 20 Days Ago
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Data entry clerk
  • Maxion Research
  • Marysville, WA FULL_TIME
  • We appreciate you checking us out! Work At Home Data Entry Research Panelist Jobs - Part Time, Full Time This work-from-home position is ideal for anyone with a diverse professional background, includ...
  • 25 Days Ago
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Research Engineer
  • Zap Energy
  • Everett, WA FULL_TIME
  • Zap Energy is currently seeking Research Engineers to help develop the next generation Z-pinch fusion device and its associated experiment systems. Research Engineers will be involved at all stages of...
  • 21 Days Ago
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R&D Research Engineering Manager
  • Zap Energy
  • Everett, WA FULL_TIME
  • Zap Energy is looking for a Research Engineering Manager who has experience managing engineering teams, the design and build of complex vacuum-mechanical assemblies and operations of large high-temper...
  • 2 Days Ago
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0 Postdoctoral Research Associate jobs found in Camano Island, WA area

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Rule 9 Intern - Summer Internship 2025
  • Snohomish County, WA
  • Everett, WA
  • Salary: $24.17 Hourly Location : Everett, WA Job Type: Internship Job Number: 2024-01731 Department: Prosecutor Division...
  • 9/24/2024 12:00:00 AM
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Part-Time Lecturer- Khoury College of Computer Sciences
  • Northeastern University
  • Seattle, WA
  • About the Opportunity The Khoury College of Computer Sciences invites applications for the position of Part-time teachin...
  • 9/24/2024 12:00:00 AM
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School of Psychology, Family, and Community Adjunct Instructors
  • Seattle Pacific University
  • Seattle, WA
  • About Seattle Pacific University: Founded in 1891 and located just minutes from downtown Seattle, SPU seeks to be a prem...
  • 9/24/2024 12:00:00 AM
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Assistant Professor Analytical Chemistry
  • Western Washington University
  • Bellingham, WA
  • Assistant Professor Analytical Chemistry Work type: TT Faculty Location: Bellingham, WA Categories: College of Science &...
  • 9/23/2024 12:00:00 AM
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IRS Internal Recent Graduate Program IT Spc (Systems Analysis/Applications Software) 9 Month Roster
  • Department Of The Treasury
  • Everett, WA
  • Summary Click on "Learn more about this agency" button below to view Eligibilities being considered and other IMPORTANT ...
  • 9/23/2024 12:00:00 AM
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PhD Researcher (Intern)
  • Centific
  • Redmond, WA
  • About Centific: Centific is a frontier AI data foundry that curates diverse, high-quality data, using our purpose-built ...
  • 9/21/2024 12:00:00 AM
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IRS Internal Recent Graduate Program IT Spc (Network Services) 9 Month Roster
  • Department Of The Treasury
  • Everett, WA
  • Summary Click on "Learn more about this agency" button below to view Eligibilities being considered and other IMPORTANT ...
  • 9/20/2024 12:00:00 AM
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Pathways Recent Graduate Prgm Info Tech Spc (Systems Analysis/Applications Software) 9 Month Roster
  • Department Of The Treasury
  • Everett, WA
  • Summary Click on "Learn more about this agency" button below to view Eligibilities being considered and other IMPORTANT ...
  • 9/20/2024 12:00:00 AM
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About Camano Island, Washington

Camano is a census-designated place (CDP) in Island County, Washington, United States. The population was 15,661 at the 2010 census. Camano is coterminous with the namesake island on which it sits. Camano (as Camano Island) has its own ZIP code (98282) but shares a post office with Stanwood, despite Stanwood's distance. Based on per capita income, one of the more reliable measures of affluence, Camano ranks 99th of 522 areas in the state of Washington to be ranked.[when?][citation needed] Camano is located at 48°11′37″N 122°29′11″W / 48.19361°N 122.48639°W / 48.19361; -122.48639 (48.193606...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Postdoctoral Research Associate jobs
$54,955 to $74,131
Camano Island, Washington area prices
were up 2.9% from a year ago
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What does a Postdoctoral Research Associate do?

Postdoctoral Research Associate in Raleigh, NC
Review scientific literature on adaptive imaging devices, image processing, machine learning and tissue clearing.
February 22, 2023
Postdoctoral Research Associate
Develop high performance lithium-ion batteries, plan and conduct research, supervise undergraduate students, prepare manuscripts for submission to peer-reviewed publications, prepare reports and papers for group meetings.
February 28, 2023
Assist with research grant proposals and provide publishable reports for conference and journal presentation.
March 27, 2023
Provides guidance to laboratory staff in one or more laboratory areas, including technicians, support and auxiliary staff.
April 02, 2023
Participate in joint projects involving faculty, junior lab personnel, and graduate students.
April 26, 2023
Demonstrated commitment to work within a diverse environment and interact openly with individuals of different backgrounds.
April 30, 2023