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Clinical Data Associate Jobs in Springfield, MA (NOW HIRING)

Determines the severity of the patient's problem based upon data collection and patient history and ... Associate's degree from an accredited relevant field and 5 years clinical experience equivalent to ...

Associate's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical ... Formore information about how we collect and store your personal data, please see ourPrivacy ...

Associate's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical ... For more information about how we collect and store your personal data, please see our Privacy ...

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How much do clinical data associate jobs pay per hour?

As of Jun 18, 2026, the average hourly pay for clinical data associate in Springfield, MA is $38.77, according to ZipRecruiter salary data. Most workers in this role earn between $29.18 and $38.75 per hour, depending on experience, location, and employer.

What are some common challenges faced by Clinical Data Associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

What are the key skills and qualifications needed to thrive as a Clinical Data Associate, and why are they important?

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What does a Clinical Data Associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What Does a Clinical Data Associate Do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

What is the difference between Clinical Data Associate vs Clinical Research Coordinator?

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

What are the most commonly searched types of Clinical Data jobs in Springfield, MA? The most popular types of Clinical Data jobs in Springfield, MA are:
What job categories do people searching Clinical Data Associate jobs in Springfield, MA look for? The top searched job categories for Clinical Data Associate jobs in Springfield, MA are:
What cities near Springfield, MA are hiring for Clinical Data Associate jobs? Cities near Springfield, MA with the most Clinical Data Associate job openings:
Infographic showing various Clinical Data Associate job openings in Springfield, MA as of June 2026, with employment types broken down into 2% As Needed, 69% Full Time, 21% Part Time, and 8% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $80,648 per year, or $38.8 per hour.
Part-Time Clinical Coordinator - Radiography

Part-Time Clinical Coordinator - Radiography

Goodwin University

East Hartford, CT

Other

Posted 20 days ago


Job description

The mission of Goodwin University is to educate a diverse student population in a dynamic environment that aligns education, commerce, and community. Our innovative programs of study prepare students for professional careers while promoting lifelong learning and civic responsibility. As a nurturing university community, we challenge students, faculty, staff, and administration to fully realize their highest academic, professional, and personal potential.

Position Description Summary/Purpose:

The newly developed Associate Degree program in Radiography is seeking a Part-Time Clinical Coordinator responsible for coordinating and overseeing the clinical education component for the five clinical semesters of the program, ensuring high educational standards and enhancing clinical training opportunities. Collaborating closely with the Radiography Program Director, this role is responsible for recruiting new clinical sites, fostering relationships with existing clinical partners, and ensuring compliance with state, college, and accreditation standards. The clinical coordinator will monitor the Joint Review Committee on Education in Radiologic Technology (JRCERT) approved clinical education facilities and their radiology staff to provide appropriate supervision of the Goodwin University radiography program students. Additionally, this staff position includes exceptional customer service, support for data management and documentation, and may include teaching one clinical and/or didactic course per semester.

Essential Job Functions/Primary Responsibilities:

(The essential functions or duties listed below are intended only as illustrations of the various types of work that may be performed. The omission of specific statements of duties does not exclude them from the position if the work is similar, related or a logical assignment to the position.)

  • Oversee the initial and on-going affiliation of clinical facilities to provide radiography rotations for all students accepted into the program
  • Oversee the process for accepted students to provide the required medical documentation to participate in clinical internships for the program.
  • Directs and coordinates all activities relative to clinical practice including coordinating the use of clinical facilities; planning schedules for clinical rotations; conducting clinical orientation sessions; providing support to clinical instructors; directing and overseeing the efficient completion of all clinical forms; and developing and upgrading clinical objectives.
  • Assist the Radiography Program Director in the assessment of clinical education and the program.
  • Assist the Radiography Program Director with the JRCERT Self-Study for initial accreditation of the program.
  • Oversee the scheduling and use of the energized radiography lab on campus for lab sessions.
  • Maintaincurrent knowledge of the JRCERT Standards and incorporatethe standards into the clinical curriculum.
  • Coordinate and supervise clinical education activities, ensuring students gain hands-on experience in a variety of healthcare settings.
  • Develop and maintain strong partnerships with clinical sites, ensuring compliance with accreditation and program standards.
  • Develop and implement clinical evaluation tools to assess student performance and competencies.
  • Perform other tasks as assigned which support the mission and initiatives of the University.
  • Conducts all work in a safe manner and all work safety practices are followed.

Other Functions:

  • Performs similar or related work as required, directed or as situation dictates.
  • Continues professional development and training; keeps current with trends.
  • Assists other department staff as needed to promote a team effort.

Knowledge, Ability and Skill:

  • Demonstrated commitment to promote diversity, equity, and inclusion, and work in an environment in which all members of the University community are treated with respect and dignity.
  • Stay current with industry trends, standards, and best practices in radiography education and clinical training.

Education, Training and Experience:

  • Bachelors Degree Required
  • Holds current American Registry of Radiologic Technologists (ARRT) certification and registration in radiography
  • Eligible to obtain State of Connecticut radiographer licensure
  • Two years' clinical experience in the professional discipline
  • One years' experience as an instructor in a JRCERT accredited programs
  • Competent in the implementationand useof the clinicalcompetency tracking system and clinical compliance tracking system

Special Requirements:

  • Courses will be offered day, evening, and weekends. The clinical coordinator will be required to work some evenings and weekends to support students.

Special Requirements:

  • Valid Drivers License & Insured Vehicle

Physical and Mental Requirements:

Work EnvironmentNone Under 1/31/3 to 2/3Over 2/3Outdoor Weather ConditionsXWork with fumes or airborne particlesXWork near moving mechanical partsXRisk of electrical shockXVibrationXPhysical ActivityNone Under 1/31/3 to 2/3Over 2/3Standing XWalkingXSittingXTalking & HearingXUsing hands/fingers to handle/feelClimbing or balancingXBending, pulling, pushingXDrivingXLifting RequirementsNone Under 1/31/3 to 2/3Over 2/3Up to 10 pounds XUp to 25 poundsXUp to 50 poundsXUp to 75 poundsXUp to 100 poundsXOver 100 poundsX

Vision requirements:

_X_ Close vision (i.e. clear vision at 20 inches or less)

___ Distance vision (i.e. clear vision at 20 feet or more)

___ Color vision (i.e. ability to identify and distinguish colors)

___ Peripheral vision (i.e. ability to observe an area that can be seen up and down or

left and right while the eyes are fixed on a given point)

___ Depth perception (i.e. three-dimensional vision, ability to judge distances and

spatial relationships)

___ No special vision requirements

(This job description does not constitute an employment agreement between Goodwin University and employee. It is used as a guide for personnel actions and is subject to change by The University as the needs of The University and requirements of the job change.)