Clinical Research Manager jobs in Marysville, WA
Clinical Research Manager manages the clinical monitoring process and the administration of clinical trials. Supervises CRAs in in-house and on-site monitoring, filing, and clinical trial administration. Being a Clinical Research Manager oversees adherence to SOPs, Good Clinical Practice and FDA regulations. Helps with the development and implementation of clinical processes, procedures, and programs. Additionally, Clinical Research Manager may require a master's degree in nursing. May require ACRP or SOCRA Clinical Research Professional exam completion. Typically reports to a director. The Clinical Research Manager manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. To be a Clinical Research Manager typically requires 5 years experience in the related area as an individual contributor. 1-3 years supervisory experience may be required. Extensive knowledge of the function and department processes. (Copyright 2024 Salary.com)
Recently Added Clinical Research Manager jobs
Senior Clinical Research Coordinator
- Innovo Research
-
Everett, WA
OTHER
-
Job Summary
The Senior CRC/Site Manager will work closely with Principal Investigators and clinical research teams to coordinate the daily operations of clinical research studies and oversee clinical research staff performing clinical functions at the designated Innovo Research partner site. Reporting will include accountability to the Sr. Director of Clinical Operations, PI, and others, as necessary. You are accountable for conduct of clinical research/trials in accordance with Good Clinical Practices (GCPs), applicable regulations and guidelines, and Standard Operating Procedures (SOPs). This individual will play a key role in facilitating the training and support of local physicians, and research staff on protocol requirements, GCP and other applicable regulatory requirements. The Senior CRC/Site Manager will be responsible for making sure that all clinical research activities are efficiently executed, conducted in a professional manner that is compliant with all human research subject regulations.
Essential Duties/Responsibilities- Oversee/assist with mentoring and training clinical research staff.
- Maintain frequent communication with research assistants and research coordinators regarding enrollment and tasks, as assigned.
- Perform clinical functions i.e. phlebotomy, monitoring vital signs on study participants, etc., when warranted; educates family and contributes to the care and evaluation of subjects, including determining preliminary inclusion/ exclusion criteria.
- Liaises with agencies, pharmaceutical companies, laboratories, vendors, equipment and supply companies as needed; oversees availability of supplies and/or equipment for studies.
- Directly coordinate regular research meetings.
- Assist the principal investigator with the management of day-to-day operations related to clinical research and subject care as necessary.
- Manage multiple concurrent trials - screening, recruiting and enrollment, perform patient/research participant scheduling, coordinate protocol related research procedures, study visits, and follow—up, collect patient/ research participant history, collect and maintain source documentation, perform data entry and query resolution, prepare IRB submissions, update required modifications, continuing reviews, and reportable events.
- Develop strong working relationships and maintain effective communication with study team members.
- Develop strong working relationships and become the point of contact for the clinic as well as the sponsor for clinic related activities.
- Completes all protocol related training and adhere to IRB approved protocol(s)
- Support the collection and review of required essential study documents and reports.
- Order supportive study supplies (e.g., contracts, IXRS, lab kits, non-clinical supply materials, imaging, and laboratory handling manuals, etc.).
- Assist in the informed consent process of research subjects.
- Support and advocate for the safety of research subjects.
- Facilitate pre-study, site qualification, study initiation, monitoring visits, and study close out activities.
- Collect, process and ship laboratory specimens.
- Comply with Innovo, Clinic, and Sponsor policies, standard operating procedures (SOPs), applicable regulatory requirements and guidelines.
- Performs all additional duties as assigned.
- At least 3-5 years of experience coordinating clinical trials, including the activities listed above.
- A Master's degree or previous management experience may substitute for one year of related experience with coordinating clinical trials.
- BS/BA in Life Science or related discipline. CCRC certification a plus.
- Previous GCP training and certification required and working knowledge of current ICH GCP guidelines and applicable regulations. Experience in a clinical setting a plus
- Demonstrated ability in positive relationship building.
- Previous experience with training and mentoring other clinical research professionals a plus.
- Strong interpersonal skills with attention to detail a must. Positive attitude and ability to interact with all levels of staff to coordinate and execute study activities.
- Demonstrated proficiency with word processing, spreadsheet, database, and presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, SharePoint) and with clinical trial master filing systems.
- Strong organization/prioritization skills for the management of multiple concurrent projects.
- An understanding of Regulatory and Central/Local ethic submission processes
- Ability to manage multiple competing priorities within various clinical trials.
- Excellent verbal and written communication skills required.
- Ability to work independently, prioritize and work with a matrix team environment is essential.
- Ability to travel for Clinic activities, attend investigator meetings or vendor visits/audits, as required.
- Competitive salary
- Health Insurance
- Dental Insurance
- Disability Insurance
- Life Insurance
- Paid Time Off
- Vision Insurance
This job operates in a professional and clinical environment with occasional visits to other Innovo Research partner sites/clinics. This role routinely uses standard office equipment such as computers, phones, and scanners. There is frequent exposure to communicable diseases, toxic substances, ionizing radiation, medicinal preparations, and other conditions common to a clinic environment. Varied activities include standing, walking, reaching, bending, and lifting. Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 50 pounds. Requires corrected vision and hearing to normal range.
Due to the nature of this position, employees are expected to work in person. This is an exempt position under the federal and state wage and hour laws, which means you are not eligible for overtime pay beyond your salary. Employees are expected to work 40 hours a week. Occasional evening and weekend work may be required as job duties demand.
The above statements are intended to describe the general nature and level of work being performed by individuals assigned to this position. They are not intended to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel. More in-depth information can be found in SOP's, working guidelines, policies, etc. Innovo Research is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Innovo are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Innovo Research will not tolerate discrimination or harassment based on any of these characteristics. In addition, Innovo will provide reasonable accommodations for qualified individuals with disabilities.
Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. - 4 Days Ago
Associate Clinical Research Coordinator
- Providence Health
-
Everett, WA
FULL_TIME
- Description The CRC1 is responsible for coordinating and maintaining diverse activities related to clinical research. This includes, but is not limited to: patient eligibility; registration/enrollment...
- 1 Day Ago
Associate Clinical Research Coordinator
- Swedish
-
Everett, WA
FULL_TIME
- DescriptionThe CRC1 is responsible for coordinating and maintaining diverse activities related to clinical research. This includes, but is not limited to: patient eligibility; registration/enrollment;...
- 4 Days Ago
Manager of Physical Therapy
- Clinical Management Consultants
-
Arlington, WA
FULL_TIME
- An incredible opportunity to become a Manager of Physical Therapy has become available in a thriving community hospital in Northwestern Washington. This medical center is integral to maintaining the h...
- 4 Days Ago
Manager Behavioral Health
- Clinical Management Consultants
-
Oak Harbor, WA
FULL_TIME
- An esteemed hospital is looking for its next Mental Health Program Manager to join its dedicated team. This pivotal role offers the opportunity to lead transformative initiatives, shaping the future o...
- 11 Days Ago
Manager Behavioral Health
- Clinical Management Consultants
-
Greenbank, WA
FULL_TIME
- An esteemed hospital is looking for its next Mental Health Program Manager to join its dedicated team. This pivotal role offers the opportunity to lead transformative initiatives, shaping the future o...
- 1 Month Ago
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0 Clinical Research Manager jobs found in Marysville, WA area
Research Associate (221400)
- Medix™
-
Everett, WA
- Animal Research Associate Do you love working with animals? Do you want to contribute to advancing human health science ...
- 5/24/2024 12:00:00 AM
Research Associate / Senior Research Associate, Biology
- Sound Biologics
-
Bothell, WA
- Title: Research Associate / Senior Research Associate, Biology Job Type: Exempt, Full-Time Salary Range: $88,000 - $112,...
- 5/24/2024 12:00:00 AM
Research Associate - 221399
- Medix™
-
Everett, WA
- About the Role: The purpose of this role is to assist and work in the discovery, development, and manufacturing of new d...
- 5/23/2024 12:00:00 AM
Senior Scientist, Potency Assays for Antibodies
- The Judge Group
-
Bothell, WA
- Do you want to join a team where the mission is meaningful, the challenges are complex, and you can directly see the res...
- 5/23/2024 12:00:00 AM
Associate Scientist / Scientist
- SystImmune
-
Redmond, WA
- Company Overview: SystImmune Inc. is a dynamic clinical-stage bio-pharmaceutical company headquartered in Redmond, WA. O...
- 5/23/2024 12:00:00 AM
Clinical Laboratory Technician onsite in Yokosuka Japan
- Arcetyp LLC
-
Seattle, WA
- Arcetyp LLC is a growing small business that provides a broad range of consulting services to US Federal Government, US ...
- 5/22/2024 12:00:00 AM
Clinical Laboratory Technician onsite in Iwakuni Japan
- Arcetyp LLC
-
Seattle, WA
- Arcetyp LLC is a growing small business that provides a broad range of consulting services to US Federal Government, US ...
- 5/22/2024 12:00:00 AM
Senior Scientist, Potency Assays for Antibodies
- Lundbeck
-
Bothell, WA
- Do you want to join a team where the mission is meaningful, the challenges are complex, and you can directly see the res...
- 5/2/2024 12:00:00 AM
About Marysville, Washington
According to the United States Census Bureau's 2010 census, Marysville has a total area of 20.94 square miles (54.2 km2)—20.68 square miles (53.6 km2) of land and 0.26 square miles (0.67 km2) of water. The city is located in the northwestern part of Snohomish County in Western Washington, approximately 35 miles (56 km) north of Seattle.:3 Marysville's city limits are generally bound to the south by Ebey Slough (part of the Snohomish River delta) and Sopher Hill Road, to the west by Interstate 5 and the Tulalip Indian Reservation, to the north by the city of Arlington, and to the east by the Ce...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Manager jobs
$107,844 to $142,880
Marysville, Washington area prices
were up 2.9% from a year ago
were up 2.9% from a year ago
What does a Clinical Research Manager do?
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