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Exercise Science Research Jobs in Dallas, TX (NOW HIRING)

Texas A&M AgriLife

Program Coordinator II

Dallas, TX · On-site

Texas A&M AgriLife Research * College of Agriculture and Life Sciences at Texas A&M University ... exercise physiology, health communications, public health, social sciences, life sciences ...

Tamus

Program Coordinator II

Dallas, TX · On-site

Texas A&M AgriLife Research * College of Agriculture and Life Sciences at Texas A&M University ... exercise physiology, health communications, public health, social sciences, life sciences ...

Equinox

Personal Trainer Internship, Plano

Plano, TX · On-site

Research the following conditions: Hypertension, Diabetes, Pregnancy, CVD with points on cause ... Exercise Science, Kinesiology, Physical Education, Personal Training, or other applicable majors ...

Yum Brands

Sr. Data Scientist

Plano, TX · On-site

$117K - $132K/yr

... exist, exercise strong judgment in choosing methods, and create or significantly improve the ... Advanced degree in Statistics, Mathematics, Economics, Data Science, Operations Research, or a ...

Pizza Hut

Sr. Data Scientist

Plano, TX

$117K - $132K/yr

... exist, exercise strong judgment in choosing methods, and create or significantly improve the ... Advanced degree in Statistics, Mathematics, Economics, Data Science, Operations Research, or a ...

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Showing results 21-40

All JobsExercise Science Research JobsExercise Science Research Jobs in Dallas, TX

Exercise Science Research information

See Dallas, TX salary details

$27.7K

$89.4K

$152.3K

How much do exercise science research jobs pay per year?

As of Aug 12, 2026, the average yearly pay for exercise science research in Dallas, TX is $89,446.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,600.00 and $97,400.00 per year, depending on experience, location, and employer.

What are some common challenges faced by professionals in exercise science research, and how can they be overcome?

Professionals in Exercise Science Research often encounter challenges such as recruiting and retaining study participants, ensuring data reliability, and managing complex interdisciplinary projects. Building strong relationships with local communities and athletic organizations can improve participant engagement. Additionally, collaborating closely with colleagues from nutrition, physiology, and medical backgrounds helps ensure comprehensive research design and analysis. Staying current with advancements in technology and research methodology also supports high-quality, impactful studies.

What is the difference between Exercise Science Research vs Exercise Physiologist?

AspectExercise Science ResearchExercise Physiologist
Required CredentialsBachelor's or Master's in Exercise Science or related field; research experience often preferredBachelor's or Master's in Exercise Physiology; certification (e.g., ACSM) often required
Work EnvironmentLaboratories, universities, research institutionsClinics, hospitals, fitness centers, sports facilities
Employer & IndustryAcademic institutions, research organizations, government agenciesHealthcare providers, fitness industry, sports teams
Common Search & Comparison IntentUnderstanding research roles in exercise scienceCareer as a practicing exercise physiologist

Exercise Science Research focuses on conducting studies to advance knowledge in exercise and human performance, often within academic or research settings. In contrast, Exercise Physiologists apply exercise principles directly to improve health and fitness in clinical or fitness environments. Both roles require related educational backgrounds but differ in daily tasks and work settings.

What are the key skills and qualifications needed to thrive as an exercise science researcher?

To thrive as an Exercise Science Researcher, you need a solid background in physiology, biomechanics, and data analysis, usually supported by a relevant degree such as a master's or PhD in exercise science or a related field. Familiarity with laboratory equipment, statistical analysis software (like SPSS or R), and research methodologies is essential. Strong analytical thinking, attention to detail, and effective communication skills are crucial for designing studies and sharing findings. These skills ensure rigorous research practices, accurate data interpretation, and impactful contributions to the advancement of exercise science.

What is exercise science research?

Exercise science research involves the systematic study of how physical activity, exercise, and sports impact human health, performance, and disease prevention. Researchers in this field investigate a range of topics including biomechanics, physiology, nutrition, psychology, and motor control. The goal is to understand how exercise affects the body and mind so that effective programs and recommendations can be developed for individuals and populations. Exercise science research is crucial for advancing knowledge in sports performance, rehabilitation, and overall health promotion.
What are popular job titles related to Exercise Science Research jobs in Dallas, TX? For Exercise Science Research jobs in Dallas, TX, the most frequently searched job titles are:
What job categories do people searching Exercise Science Research jobs in Dallas, TX look for? The top searched job categories for Exercise Science Research jobs in Dallas, TX are:
What cities near Dallas, TX are hiring for Exercise Science Research jobs? Cities near Dallas, TX with the most Exercise Science Research job openings:
Exercise Science Research jobs near you
Infographic showing various Exercise Science Research job openings in Dallas, TX as of August 2026, with employment types broken down into 83% Full Time, 4% Part Time, and 13% Contract. Highlights an 96% In-person, and 4% Remote job distribution, with an average salary of $89,446 per year, or $43 per hour.

Clinical Research Coordinator I

Pinnacle Clinical Research, LLC

Dallas, TX • On-site

$24 - $32/hr

Full-time

Re-posted 29 days ago

Job description

Come join our team and make a difference as we blaze the way into the future of medical discovery through world-class clinical research. At Dallas Research Institute, we are committed to driving innovation and advancing medical knowledge. Through our rigorous research studies, we strive to unlock breakthroughs that have the potential to transform patient care and improve lives. We pride ourselves on conducting high quality research as a complement to the medical care that our volunteers receive from their routine care center. Together, we will raise awareness about the importance of clinical research and its role in shaping the future of healthcare. Be a part of the discovery!
Summary: The Clinical Research Coordinator I will manage the day-to-day operations of assigned clinical trials and ensure that pre-established work scope, study protocol, and regulatory requirements are followed. They will recruit and screen study participants, document and report on the daily operations of a study, and participant status. This person must be able to understand clinical trial priorities and establish a workflow to complete all required activities promptly. This position is responsible for a broad range of duties involving confidential information. Strong communication and organizational skills are essential, along with a proactive, problem-solving mindset.
The Clinical Research Coordinator I must be organized, excel at multi-tasking, detail-oriented, an excellent communicator, and be able to provide high-quality participant care. This person will collaborate very closely with other members of the team, pharmaceutical sponsors, and external vendors, and, therefore, must be highly collaborative, goal-oriented, flexible, and communicative. An ideal candidate will be responsive, thoughtful, empathetic, initiative-taking, a team player, and able to manage multiple projects effectively and efficiently. This role reports directly to the Clinical Operations Manager.
Duties and Responsibilities:
Clinical Trial Execution:
  • Exercise judgement within the allowable limits defined within clinical trial protocols, standard operating procedures, and the direction from the study investigator, Operations Manager, and Site Director or Regional Director
  • Maintain participant privacy and data confidentiality, complying with the appropriate sponsor requirements and regulations, which include the FDA, ICH GCP, HIPAA, institutional review board determinations, and institutional policies and procedures
  • Complete study-directed assessments with participants, which may include, but are not limited to, informed consent, medical history, adverse events, Fibroscan, memory screen, test article handling, appointment scheduling, records review, treatment coordination, and collecting vital signs
  • Complete documentation and data management related tasks as instructed by supervisor and compliance leadership in accordance with GCP and other regulatory guidelines
  • Function as a liaison with pharmaceutical sponsors and external vendors, including but not limited to, participating in monitoring visits and audits
  • Responsible for participant management and engagement from the recruitment of study participants to study completion as applicable.
  • Respond to internal and external requests for information promptly
  • Identify opportunities to improve participant care and satisfaction
  • With a solutions-oriented and collaborative mindset, resolve study-related challenges within a reasonable time set by the supervisor
  • Establish, develop, and maintain productive relationships with internal and external personnel to achieve a high standard of research outcomes.
  • Coordinate multiple projects with competing priorities and deadlines as needed, based on clinical trial protocol directives and study volume
  • Attends the investigator’s meeting, pre-study site visit, study initiation visit, and all other study-related visits hosted by monitors or sponsor representatives as appropriate
  • Track enrollment status reports to ensure study sites stay on track to meet enrollment goals
  • Track study-specific status reports to ensure all required information regarding site issues, deviations, and CRF status is kept current
Administration:
  • Create memos, emails, and letters related to study activities
  • Create and maintain reports and/or spreadsheets as requested
  • Assist regulatory personnel in maintaining study documents and ensure electronic regulatory documents are saved and uploaded appropriately
  • Responsible for reporting safety information to regulatory agencies
  • Perform quality checks on source documents specific to the study
  • Assist with the Corrective and Preventive Action Plan (CAPA) process as needed
Duties, responsibilities, and activities may change, or new ones may be assigned at any time.
Education / Experience:
  • High school diploma or general education degree (GED) required
  • Bachelor’s Degree in a scientific area of study preferred or equivalent combination of education, training, and experience, or promotion internally from the Research Assistant role
  • 1 year of experience as a Clinical Research Assistant or Coordinator
  • 1-2 years of experience in Clinical Research
  • Proficient in all Microsoft Office applications and Clinical Research IO (CRIO) or equivalent CTMS
  • Must have strong knowledge of ICH/GCP guidelines
  • Must complete GCP training before interacting with participants and must recertify every 2 years or as applicable
  • Trained and certified in the administration of Fibroscan and memory screens as required by study portfolio and individual experience. Training to be provided
  • Must have basic life support (BLS) training, provided during onboarding
  • Demonstrated organizational skills and outstanding time management, including keen attention to detail, with the ability to track multiple projects at one time
  • Strong written and oral communication skills
  • Knowledge of basic medical terminology
  • Possess impeccable integrity and personal and professional values that are consistent with PCR’s high standards and mission
  • Comply with the company policies, code of ethics, and guiding values always
  • Proficient in English and Spanish required
Supervisory Responsibilities: None
Certificates and Licenses: Valid Driver’s License
Knowledge, Skills, and Other Abilities:
  • Must be able to effectively communicate with all levels of internal and external contacts
  • Demonstrated ability to manage a high-volume workload with multiple clinical trials while maintaining accuracy and compliance.
  • Ability to work independently and multitask in a fast-paced team environment
  • Strong people skills, including the ability to interact with individuals from diverse backgrounds and to oversee confidential matters and sensitive information with discretion and judgment
  • Must possess a positive, friendly, and professional demeanor, particularly when interacting with research participants
  • Must be able to work independently and collaborate with a team
  • Ability to interpret clinical research protocols
  • Strong problem-solving and decision-making skills, particularly when under pressure
  • Proactive at identifying, addressing, and solving issues in real time
  • Energetic self-starter, results-oriented, and able to work effectively in an entrepreneurial environment
Work Environment and Physical Demands:
The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
  • Work is performed in an office/laboratory and/or a clinical environment.
  • Exposure to biological fluids and/or bloodborne pathogens.
  • Personal protective equipment is required, such as protective eyewear, garments, and gloves.
  • Occasional travel may be required, domestic and/or international.
  • Ability to work in an upright and/or stationary position for 6-10 hours per day.
  • Frequent mobility required.
  • Occasional squatting, kneeling, or bending.
  • Light to moderate lifting and carrying (or otherwise moving) objects, including medical equipment with a maximum lift of 20-50 lbs.
Dallas Research Institute is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, disability, gender, national origin, age, genetic information, military or veteran status, sexual orientation, gender identity, marital status, or any other protected Federal, State/Province, or Local status unrelated to the performance of the work involved.

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