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High Point Clinical Trials Jobs (NOW HIRING)

BANDANA

Clinical Trials Nurse - GU Renal

Manhattan, NY · Hybrid

$41.97/hr

... with high energy and enthusiasm. - A good decision-maker, with shown success at making timely ... clinical trials in general and the specifics of the proposed clinical trial. - Provide direct ...

Advocate Aurora Health

Department: 36367 High Point Medical Center - Radiology: Special Studies Status: Full time Benefits ... of clinical trials and research studies, with Wake Forest University School of Medicine serving as ...

Agilent

OR · On-site

... Serve as main point of contact for internal and external study stakeholders ... high standards of performance from project team Lead and work with the project team to identify ...

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High Point Clinical Trials information

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How much do high point clinical trials jobs pay per hour?

As of Jun 8, 2026, the average hourly pay for high point clinical trials in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in clinical trial management at an organization like High Point Clinical Trials, and why are they important?

To excel in clinical trial management, you need a solid background in life sciences, clinical research, and regulatory compliance, often supported by a relevant degree and certifications such as CCRA or ACRP. Familiarity with electronic data capture systems (EDC), clinical trial management systems (CTMS), and Good Clinical Practice (GCP) guidelines is crucial. Strong organizational skills, attention to detail, and effective communication are vital soft skills for coordinating studies and ensuring protocol adherence. These competencies ensure that trials are conducted efficiently, ethically, and in accordance with regulatory standards, leading to reliable study outcomes.

What are High Point Clinical Trials?

High Point Clinical Trials typically refers to a research organization or facility in High Point, North Carolina, that conducts clinical research studies to test the safety and effectiveness of new medications, treatments, or medical devices. These clinical trials involve volunteers who participate under the supervision of medical professionals and according to strict protocols. The data collected from these trials helps regulatory agencies determine whether a new treatment should be approved for use in the general population. Participation in clinical trials can provide access to cutting-edge therapies and contribute to advancements in medical science.

What are some common challenges faced when working in clinical trials at High Point Clinical Trials, and how can new team members effectively navigate them?

Working in clinical trials at High Point Clinical Trials often involves managing tight timelines, ensuring strict regulatory compliance, and coordinating across multidisciplinary teams such as data management, regulatory affairs, and clinical operations. New team members may initially find it challenging to balance documentation requirements with participant care and protocol adherence. To navigate these challenges, it’s helpful to proactively communicate with colleagues, seek guidance from experienced team members, and stay updated on industry best practices and company protocols. Embracing a collaborative mindset and continuous learning will help you adapt quickly and contribute effectively to the success of the trials.

What is the difference between High Point Clinical Trials vs Clinical Research Coordinator?

AspectHigh Point Clinical TrialsClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications like CCRP or CCRC are common
Work EnvironmentConducts clinical trials at research sites, hospitals, or clinicsWorks at research sites, hospitals, or clinics managing trial activities
Employer & IndustryPharmaceutical companies, contract research organizations, academic institutionsResearch sites, hospitals, pharmaceutical companies

High Point Clinical Trials and Clinical Research Coordinators both work in clinical research settings, often at the same sites. The main difference lies in roles: High Point Clinical Trials may be a specific organization conducting trials, while Clinical Research Coordinators manage daily trial activities. Both roles require similar credentials and work environments, making them closely related in the clinical research industry.

More about High Point Clinical Trials jobs
What states have the most High Point Clinical Trials jobs? States with the most job openings for High Point Clinical Trials jobs include:
What job categories do people searching High Point Clinical Trials jobs look for? The top searched job categories for High Point Clinical Trials jobs are:
High Point Clinical Trials jobs near you
Infographic showing various High Point Clinical Trials job openings in the United States as of May 2026, with employment types broken down into 3% As Needed, 73% Full Time, 18% Part Time, 3% Temporary, and 3% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Quality Control Specialist - Clinical Trials

SRA Trials

Miami, FL

$25 - $30/hr

Full-time

Medical, Dental, Vision, Life, PTO

Posted 13 days ago

Job description

Quality Control Specialist - Clinical Trials
Suncoast Research Associates is a privately owned and operated research organization established in 2018. We help volunteers get involved in clinical trials which allow patients to play a more active role in their own health care, gain access to new research treatments before they are widely available, and help others by contributing to medical research. Our company works with all major pharmaceutical companies and conducts studies in a myriad of therapeutic areas. We are located in Doral, Florida and do not offer remote work.
Key Responsibilities
  • Demonstrate exceptional attention to detail, organization, and accountability while managing multiple priorities in a fast-paced clinical research environment.
  • Independently review and interpret study protocols, amendments, investigator brochures, and study manuals to ensure accurate application of study requirements.
  • Perform quality control (QC) review of clinical data across multiple protocols and therapeutic areas, including concurrent enrolling studies.
  • Conduct thorough review of medical records, source documents, and study charts in collaboration with Investigators and site staff to ensure data integrity and protocol compliance.
  • Complete accurate and timely data review within electronic data capture (EDC) systems (e.g., Inform, Medidata Rave, Veeva Vault).
  • Ensure adherence to sponsor and study timelines for data entry, query resolution, and database updates in accordance with SRA or sponsor expectations.
  • Perform routine and targeted quality assurance checks to verify that study processes and data meet protocol, GCP, and regulatory standards.
  • Identify, document, and escalate data discrepancies, deviations, and quality issues; support root cause analysis and corrective and preventive actions (CAPA).
  • Analyze data trends and patterns to identify opportunities for process improvement and enhanced data quality.
  • Collaborate cross-functionally with study coordinators, investigators, monitors, and sponsors to resolve data queries and quality concerns efficiently.
  • Support and coordinate monitoring visits, audits, and inspections, ensuring all required documentation is accurate, complete, and audit-ready.
  • Respond to and help resolve data queries generated by monitors, auditors, or other reviewers in a timely and effective manner.
  • Maintain accurate and comprehensive documentation of QC activities, findings, and resolutions.
  • Provide administrative and clerical support, including order entry and study-related documentation tasks as needed.
  • Communicate professionally and effectively with internal teams, sponsors, CROs, and external vendors.
Required skills and abilities
  • Strong organizational skills with the ability to prioritize tasks and meet deadlines.
  • Proficient in data collection, analysis, and reporting using tools such as Excel and pivot tables.
  • Attention to detail and a high level of accuracy in transcribing information.
  • Basic math skills for performing calculations related to quality assurance.
  • Excellent communication skills, both written and verbal.
  • Proficient in Microsoft Office suite (Word, Excel, PowerPoint).
  • Previous experience in quality assurance or related role is preferred.
Benefits:
  • Dental insurance
  • Health insurance
  • Life insurance
  • Paid time off
  • Vision insurance
Schedule:
  • 8 hour shift
  • Monday to Friday
  • Onsite (no remote work)

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