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Temporary Spss Data Entry Jobs in Oregon (NOW HIRING)

AllSTEM Connections

Sales Data Analyst

Medford, OR · On-site

$70K - $80K/yr

QUALIFICATIONS FOR ENTRY: KNOWLEDGE OF: * Data processing methods, relational tables, procedures ... For temporary assignments lasting 13 weeks or longer, AllSTEM Connections is pleased to offer major ...

Labcorp

Specimen Accessioner

Portland, OR · On-site

$17 - $20/hr

Data entry of patient information in an accurate and timely manner * Resolve and document any ... Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees ...

Labcorp

Specimen Accessioner

Portland, OR

$16.75 - $19.75/hr

Data entry of patient information in an accurate and timely manner  * Resolve and document any ... Temporary employees are only eligible to participate in the 401(k) Plan. For more detailed ...

Aston Carter

Accounts Payable Clerk

Newberg, OR · On-site

$22/hr

Perform data entry for accounts payable transactions, including invoice coding, matching, and ... If eligible, the benefits available for this temporary role may include the following: • Medical ...

Aston Carter

Accounts Payable Clerk

Newberg, OR

$22 - $22.60/hr

Perform data entry for accounts payable transactions, including invoice coding, matching, and ... If eligible, the benefits available for this temporary role may include the following: * Medical ...

Labcorp

Specimen Accessioner

Portland, OR · On-site

$17 - $20/hr

Data entry of patient information in an accurate and timely manner * Resolve and document any ... Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees ...

Labcorp

Specialty Lab Assistant

Portland, OR

Scan and/or data entry of specimen and patient information * Ensure all lab equipment is working ... Temporary employees are only eligible to participate in the 401(k) Plan. For more detailed ...

Labcorp

Specialty Lab Assistant

Portland, OR · On-site

Scan and/or data entry of specimen and patient information * Ensure all lab equipment is working ... Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees ...

Jireh Semiconductor

Temp to Hire Fab Tech

Hillsboro, OR · On-site

$20/hr

Responsible for accurate entry of that data into workstream system for assessment of processing ... Temp to hire opening 6-12 months, conversion based on company needs. This position will be staffed ...

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Temporary Spss Data Entry information

What is a temporary SPSS data entry job?

Temporary SPSS data entry jobs involve entering, cleaning, and managing data using IBM SPSS software for a limited period, often on a contract or project basis. These roles typically require strong attention to detail and familiarity with SPSS software, as well as the ability to accurately input large volumes of data. Temporary SPSS data entry professionals may work in fields such as research, healthcare, education, or marketing, supporting teams with essential data preparation tasks for analysis. The work may be onsite or remote, depending on the employer’s needs.

What skills and qualifications are needed for a temporary SPSS data entry job?

To thrive in a Temporary SPSS Data Entry role, you need strong attention to detail, proficiency in data entry, and a basic understanding of statistical concepts, often supported by experience with data management. Familiarity with SPSS software is essential, and knowledge of Excel or other database systems is often required. Accuracy, time management, and the ability to work independently are key soft skills that distinguish top performers. These skills and qualities are vital for ensuring reliable data input, minimizing errors, and supporting accurate analysis in research or business projects.

What are common challenges in a temporary SPSS data entry job, and how can they be managed?

In a Temporary SPSS Data Entry role, common challenges include ensuring data accuracy while working under tight deadlines and managing large volumes of information. Attention to detail is crucial, as input errors can impact data analysis outputs. To manage these challenges, it's important to regularly validate entries, use SPSS’s built-in data validation tools, and communicate with team members to clarify any ambiguous data points. Staying organized and following consistent workflows can also help maintain accuracy and efficiency throughout the assignment.

What is the difference between Temporary Spss Data Entry vs Temporary Data Analyst?

AspectTemporary Spss Data EntryTemporary Data Analyst
CredentialsBasic computer skills, familiarity with SPSSDegree in statistics, data science, or related field
Work EnvironmentData entry settings, offices, remoteData analysis projects, offices, remote
Industry UsageResearch firms, academic institutions, market researchBusiness, healthcare, finance, research

Temporary Spss Data Entry primarily involves inputting data into SPSS software with minimal analysis, focusing on accuracy and speed. Temporary Data Analysts perform more complex data interpretation, statistical analysis, and reporting. While both roles require familiarity with data tools, Data Analysts typically have advanced credentials and handle broader responsibilities.

What cities in Oregon are hiring for Temporary Spss Data Entry jobs?

Cities in Oregon with the most Temporary Spss Data Entry job openings:

Temporary Spss Data Entry jobs near you

TI Clinical Research Coordinator

Oregon Health & Science University

Portland, OR • On-site

$48K - $77K/yr

Full-time

Re-posted 17 days ago

Oregon Health & Science University rating

8.1

Company rating: 8.1 out of 10

Based on 95 frontline employees who took The Breakroom Quiz

163rd of 620 rated colleges and universities

Job description

Department Overview
The Clinical Trials Unit supports the vision of the Division of Cardiovascular Medicine, the Knight Cardiovascular Institute (KCVI) and OHSU Health to provide Oregonians with state-of-the-art facilities and outstanding staff to advance treatments for cardiovascular diseases. KCVI and OHSU Health proudly collaborate to support clinical research and bring the future of cardiovascular care to the present. Our clinic, located on the South waterfront in CHH1, supports the complex care initiative and the Healthcare mission's priorities, while the CTU provides in patient trial opportunities and procedural care on OHSU main campus as well. Our unit provides the physical infrastructure to perform pharmacological and medical device trials including trials which require infusions, genetic trials, device implants, and cutting-edge imaging.
The Knight Cardiovascular Institute Clinical Research Assistant II (Assistant Coordinator) is responsible for various duties related to clinical trials. They will assist the study coordinators in supporting patient visits, assists in data collection and entry for the sponsor, and coordinates patient travel to ensure study subjects are able to meet their visits. This position will primarily support our Cardiomyopathy research team within the division of Cardiology, they may be reassigned secondary duties to support other sections within the Cardiovascular Medicine Clinical Trials Unit and Knight Cardiovascular Institute. This is an onsite role with limited hybrid opportunities.
Function/Duties of Position
  • Always promotes the mission of the Knight Cardiovascular Institute through our Professional Standards of timely Customer Service, Reliability, Productivity, Professionalism, Accuracy, Timeliness, Integrity, and Problem-Solving.
  • Responsible for many aspects of clinical trial operations from site initiation visit to closeout and assuring appropriate conduct of protocols to meet FDA guidelines. This includes but is not limited to:
    • Works in collaboration with study coordinator to maintain and file regulatory and study documents of active trials to meet study requirements
    • Create a weekly task list of outstanding items for review to ensure data entry to EDC is captured within obligatory time frames
    • Collection and transcription of all laboratory and imaging data with guidance from the coordinator as needed.
    • Data entry of visit data into central data repositories (eCRIS, internal subject trackers, etc.)
    • Addressing all imaging and laboratory queries in sponsor ERT
    • Maintaining laboratory reporting and signature requests from the PI
  • Responsible for elements of patient visits including but not limited to:
  • Work with coordinator in planning visit activities and scheduling participant appointments
    • Take point on patient scheduling
    • Coordination of patient travel
    • Prepping any necessary documents prior to the visit
    • Responsible for communicating with patients regarding scheduled appointments
    • Work with coordinator in collaborating with ancillary departments to make sure all patients receive timely ECHO's, Imaging, vitals (blood pressure, temp, respirations, height, weight) or other study related tasks as needed.
    • Independently provide follow up for subjects who are no longer receiving treatment in the form of phone calls or clinic visits.
    • Work with monitoring groups to ensure all data is captured as per protocol
  • Assist the Clinical Trial Leadership, coordinators, or Principal Investigator with other research related projects and administrative/office related duties as needed
  • Assist manager and coordinator as needed in supporting sponsor visits (i.e. proctoring visits, monitoring, site initiation, etc.)

Required Qualifications
  • Bachelor's in relevant field OR
  • Associate's AND 2 years of relevant experience OR
  • 3 years of relevant experience OR
  • Equivalent combination of training and experience
  • Ability to prioritize multiple tasks at one time
  • Must have excellent communication, analytical and organizational skills: both written and verbal.
  • Ability to work independently and as part of a team while being collaborative in resolving problems.
  • Must be proficient with computers running Windows and PC applications e.g. MS Excel, Oracle, Access, Word and PowerPoint).
  • Must have demonstrated excellent customer service skills both on the phone and in person.
  • Demonstrated ability to work with a variety of diverse individuals and personalities.
  • Must possess energy and drive to coordinate multiple projects simultaneously.
  • Ability to use tact and diplomacy to maintain effective working relationships
  • Ability to perform the job duties with or without accommodation.

Preferred Qualifications
  • Bachelor's degree with coursework in Science
  • At least one year general office experience
  • Knowledge of cardiology. Managing Access database or similar database.
  • Microsoft office, medical terminology, analytical skills, trouble shooting skills. Ability to work independently as well as within a team environment.
  • BLS

Additional Details
Location: Marquam Hill & South Waterfront Campus
Schedule: Monday - Friday, 6am - 6pm primary business hours with variability depending on clinical schedules with occasional evenings & weekend work to meet project deadlines/goals. As a salaried employee assistant coordinators are expected to flex their time in conjunction with OHSU policy; this may mean working more than 40 hours in a week and then less another.
Must be able to travel to all KCVI worksite locations, including potentially using the tram numerous times each day. Will work with human biological samples, including samples which may contain infectious disease. Research assistant Coordinator may be expected to travel to conferences, new study meetings. Clinical Research Assistant Coordinator is required to use Personal Protective Equipment (gloves, masks, etc.) as required to maintain a safe and healthy clinical research environment. Additional safety training may be required to work in clinical research. Position requires ability to focus in a busy cubicle environment with multiple distractions. Position requires successful completion of BLS certification.
This is a patient facing on-site roll. Limited remote work is approved on an as needed basis by Clinical Trial Administrator. All obligations to clinical schedules and security of paper PHI and clinical trials regulations must be maintained at all times - this severely restricting the ability to conduct work remotely.
Why apply to OHSU?
We are Oregon's only public academic health center. In addition to caring for patients, we lead groundbreaking research. We also train the next generation of health care professionals. As Portland's largest employer, we give you opportunities to learn and advance in a system of hospitals and clinics across Oregon and Southwest Washington.
All are welcome. OHSU welcomes people of all ages, ethnicities, genders, national origins, religions and sexual orientations. We are striving to build an anti-racist, multicultural institution and encourage people with diverse backgrounds to apply. To request reasonable accommodation, contact askhr@ohsu.edu

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About Oregon Health & Science University

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Oregon Health & Science University (OHSU) is a distinguished institution under the industry of higher education and healthcare, specifically in the field of medical science. Based in Portland, Oregon, US, it maintains a reputation for promoting research, teaching, patient care, and outreach. Established in 1887, OHSU has continually sought to redefine the parameters of healthcare delivery and biomedical discovery through its expansive catalog of programs and initiatives. A galvanizing mission drives OHSU: to improve the health and quality of life for all Oregonians through excellence, innovation, and leadership in health care, education, and research.

Industry

Colleges, universities, and professional schools

Company size

10,000+ Employees

Headquarters location

Portland, OR, US

Year founded

1887

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