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Part Time Clinical Research Jobs in Spring, TX (NOW HIRING)

IQVIA

Clinical Trial Nurse

Houston, TX

$50 - $60/hr

... part-time clinicians, or nurses looking to supplement their income while expanding their experience in clinical research. What You'll Do * Conduct in-home visits with clinical trial patients.

IQVIA

MedTech Part Time Clinical Consultant

Houston, TX · On-site

$60/hr

... clinical research services, commercial insights and healthcare intelligence to the life sciences ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

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All JobsClinical Research JobsPart Time Clinical Research JobsPart Time Clinical Research Jobs in Spring, TX

Part Time Clinical Research information

See Spring, TX salary details

$7

$20

$41

How much do part time clinical research jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for part time clinical research in Spring, TX is $20.21, according to ZipRecruiter salary data. Most workers in this role earn between $15.38 and $23.12 per hour, depending on experience, location, and employer.

Which is better, CRC or CRA?

In clinical research, a Clinical Research Coordinator (CRC) manages daily trial activities at the site level, while a Clinical Research Associate (CRA) monitors multiple sites to ensure protocol compliance. Both roles are essential, with CRCs focusing on participant interaction and data collection, and CRAs overseeing site performance and regulatory adherence; the choice depends on career interests and desired responsibilities.

How much does a CRC make?

A Clinical Research Coordinator (CRC) in Houston typically earns between $50,000 and $70,000 annually, depending on experience, certifications, and the complexity of trials managed. Part-time CRCs may earn proportionally less based on hours worked, with hourly rates generally ranging from $20 to $35. Experience with clinical trial management systems and regulatory knowledge can influence salary levels.

What are the key skills and qualifications needed to thrive as a Part Time Clinical Research professional, and why are they important?

To excel as a Part Time Clinical Research professional, you need a foundational understanding of clinical research methods, data collection, and regulatory guidelines, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification are typically required. Attention to detail, strong organizational skills, and effective communication help you manage multiple tasks and collaborate with research teams. These competencies ensure accurate data handling, regulatory compliance, and the smooth execution of research studies.

What is the difference between Part Time Clinical Research vs Part Time Clinical Research Coordinator?

AspectPart Time Clinical ResearchPart Time Clinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldRequires a bachelor's degree; certification as a CRC is common
Work EnvironmentResearch sites, hospitals, clinics, or pharmaceutical companiesResearch sites, hospitals, clinics, often overseeing study activities
Employer & Industry UsageUsed across research organizations, biotech, pharmaPrimarily employed by research sites and clinical trial sponsors
Common Search & ComparisonOften compared for entry-level roles in clinical researchCompared for roles involving study coordination and participant management

Part Time Clinical Research roles focus on supporting clinical studies, often involving data collection and patient interactions. Part Time Clinical Research Coordinators have additional responsibilities in managing study protocols and participant coordination. Both roles require relevant education and certifications, but Coordinators typically have more oversight duties.

Can you be a CRA with no experience?

Entering a Clinical Research Associate (CRA) role typically requires some background in clinical trials, healthcare, or related fields, but entry-level positions may be available for candidates with strong organizational skills and relevant certifications such as GCP training. Most employers prefer candidates with some experience or education in clinical research, though training programs and internships can provide a pathway for those without prior experience.

How to take part in clinical research?

To participate in clinical research as a part-time clinical research worker, you can search for open positions at research institutions, hospitals, or clinical trial companies. Requirements often include relevant education or experience, and some roles may require certification or training in Good Clinical Practice (GCP). Applicants typically need to complete an application process and may undergo background checks or interviews.

What are some common challenges faced in part-time clinical research roles, and how can they be managed?

Part-time clinical research professionals often encounter challenges balancing project deadlines with limited working hours, as studies may require timely data collection and reporting. Effective communication with the research team and proactive scheduling can help ensure tasks are completed efficiently. Additionally, staying organized and regularly updating project management tools can aid in tracking progress and maintaining compliance with protocols. Building strong relationships with full-time staff also supports seamless collaboration and knowledge sharing across shifts.

What is a part-time clinical research position?

A part-time clinical research position involves assisting with the planning, implementation, and monitoring of clinical trials or studies on a reduced or flexible schedule, typically less than 40 hours per week. These roles may include tasks such as data collection, patient recruitment, regulatory documentation, and supporting principal investigators. Part-time clinical research jobs are common in hospitals, universities, and pharmaceutical companies, and they offer opportunities for students, healthcare professionals, or individuals seeking flexible work arrangements.
What are the most commonly searched types of Clinical Research jobs in Spring, TX? The most popular types of Clinical Research jobs in Spring, TX are:
What job categories do people searching Part Time Clinical Research jobs in Spring, TX look for? The top searched job categories for Part Time Clinical Research jobs in Spring, TX are:
What cities near Spring, TX are hiring for Part Time Clinical Research jobs? Cities near Spring, TX with the most Part Time Clinical Research job openings:
Part Time Clinical Research jobs near you
Infographic showing various Part Time Clinical Research job openings in Spring, TX as of June 2026, with employment types broken down into 2% As Needed, 90% Full Time, 4% Part Time, and 4% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $42,039 per year, or $20.2 per hour.
Clinical Research Principal Investigator - Neurologist

Clinical Research Principal Investigator - Neurologist

Alcanza Clinical Research

Katy, TX • On-site

$42K - $43K/yr

Part-time

Medical, Dental, Vision, Life, Retirement

Posted 15 days ago

Job description

Clinical Research Principal Investigator - Neurologist
Department: Operations
Employment Type: Part Time
Location: Olympus - Katy, TX
Reporting To: Alberto Blanco
Description
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes. Working with a local and central team drives clinical oversight and the quality of the assigned studies at the site.
Key Responsibilities
Essential Job Duties:
  • Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes
  • Overall site leadership with a focus on enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance
  • Evaluates and assesses participants to ensure only eligible participants enroll into the trials.
  • Participates and engages in successful delivery and retention of study participants.
  • Interacts positively and collaboratively with sponsors, clients and team members.
  • Practices attention to detail in recording data and participant information, following protocol guidelines and GCPs.
  • Actively involved in protocol training for staff.
  • Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues.
  • Perform other duties as assigned, requested, or required based on the needs of the participants, protocols and/or company.

Skills, Knowledge and Expertise
Minimum Qualifications: MD or DO degree, an active physician license (in good standing) in the state of practice for this role is required. Clinical Research experience is required. Board certification in neurology is required.
Required Skills:
  • Clinical procedures based on area of specialty.
  • Proficiency with computer applications such as MS Office, electronic health records, and web applications, and the ability to type proficiently (40+ wpm).
  • Must possess strong organizational skills, attention to detail, and math proficiency.
  • Well-developed written and verbal communication skills. Bi-lingual (English / Spanish) proficiency is highly preferred.
  • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, employees, subjects, managers and external customers.
  • Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.
  • Ability to be professional, respectful of others, self-motivated, and exemplify a strong work ethic.
  • Must possess a high degree of urgency, self-motivation, integrity and dependability.
  • Ability to work independently to identify problems and implement solutions.
  • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

Benefits
  • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.
  • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.

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