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Jobs at ObjectiveHealth (Now Hiring) — 12 open

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Clinical Research Coordinator II

Little Rock, Arkansas, United States · On-site

Mid level$14M raised

Description Clinical Research Coordinator II Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator II. The ideal candidate will possess 3+ year…

Skills: Clinical Research Coordination, Patient Care, IRB Protocol Management, Patient Screening, Patient Randomization

ObjectiveHealth logoObjectiveHealth

Clinical Research Data Entry Specialist

South Bend, Indiana, United States · On-site

Entry level$14M raised

Description Clinical Research Data Entry Specialist (Onsite) The Clinical Research Data Entry Specialist is responsible for accurately entering, reviewing, and maintaining clinical trial data in EDC systems. This role su…

Skills: Data Entry, Electronic Data Capture (EDC), Clinical Research, Good Clinical Practice (GCP), Medical Record Review

ObjectiveHealth logoObjectiveHealth

Clinical Research Coordinator II

Dallas, Texas, United States · On-site

Mid level$14M raised

Description Clinical Research Coordinator II - Relocation to Amarillo, TX Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator II. The ideal c…

Skills: Clinical Research Coordination, Patient Care, IRB Protocol Management, Patient Screening, Patient Randomization

ObjectiveHealth logoObjectiveHealth

Clinical Research Coordinator I

Springboro, Ohio, United States · On-site

Entry level$14M raised

Description Clinical Research Coordinator I Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator. The ideal candidate will possess certificati…

Skills: Patient Care, Phlebotomy, Clinical Trial Protocol, Patient Screening, Randomization

ObjectiveHealth logoObjectiveHealth

Clinical Research Coordinator I

Laurel, Maryland, United States · On-site

Mid level$14M raised

Description Clinical Research Coordinator I Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator. The ideal candidate will possess certificati…

Skills: Patient Care, Clinical Trial Protocol, Patient Screening, Randomization, Patient Enrollment

ObjectiveHealth logoObjectiveHealth

Clinical Research Sub-Investigator (NP/PA)

Richmond, Virginia, United States · On-site

Mid level$14M raised

Description Clinical Research Sub-Investigator (NP/PA) - Part-time ObjectiveHealth is seeking a licensed Nurse Practitioner (NP) or Physician Assistant-Certified (PA-C) to serve as a Sub-Investigator at our Richmond, VA …

Skills: Clinical Research, Patient Assessment, Medical Oversight, GCP Compliance, ICH Guidelines

ObjectiveHealth logoObjectiveHealth

Clinical Research Coordinator II

Amarillo, Texas, United States · On-site

Mid level$14M raised

Description Clinical Research Coordinator II Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator II. The ideal candidate will possess 3+ year…

Skills: Clinical Research Coordination, Patient Care, IRB Protocol Management, Patient Screening, Patient Randomization

ObjectiveHealth logoObjectiveHealth

Clinical Research Sub-Investigator (NP/PA)

Springboro, Ohio, United States · On-site

Mid level$14M raised

Description Clinical Research Sub-Investigator (NP/PA) ObjectiveHealth is seeking a licensed Nurse Practitioner (NP) or Physician Assistant-Certified (PA-C) to serve as a Sub-Investigator at our Dayton, OH research site.…

Skills: Clinical Research, Patient Assessment, Protocol Compliance, Medical Oversight, GCP

ObjectiveHealth logoObjectiveHealth

Cinical Research Coordinator I

Amarillo, Texas, United States · On-site

Entry level$14M raised

Description Clinical Research Coordinator I Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator. The ideal candidate will possess certificati…

Skills: Patient Care, Phlebotomy, Clinical Trial Protocol, Patient Screening, Randomization

ObjectiveHealth logoObjectiveHealth

Clinical Research Coordinator I

Sparta, New Jersey, United States · On-site

Entry level$14M raised

Description Clinical Research Coordinator I Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator. The ideal candidate will possess certificati…

Skills: Patient Care, Phlebotomy, Clinical Trial Protocol, Patient Screening, Randomization

ObjectiveHealth logoObjectiveHealth

Clinical Research Coordinator I

Creve Coeur, Missouri, United States · On-site

Entry level$14M raised

Description Clinical Research Coordinator I Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator. The ideal candidate will possess certificati…

Skills: Patient Care, Phlebotomy, Clinical Trial Protocol, Patient Screening, Randomization

ObjectiveHealth logoObjectiveHealth

Clinical Research Coordinator I - Bilingual (Spanish)

Laurel, Maryland, United States · On-site

Entry level$14M raised

Description Clinical Research Coordinator I - Bilingual (Spanish) Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator. The ideal candidate wi…

Skills: Patient Care, Phlebotomy, Clinical Trial Protocol, Patient Screening, Patient Enrollment

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Clinical Research Coordinator II

ObjectiveHealth

Little Rock, Arkansas, United States • On-site

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Mid level

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  • Full-time
  • 401(k) With Company Match, Short-Term Disability, Long-Term Disability, Health Savings Account, Flexible Spending Account, Health Insurance
  • Posted 3d ago
  • ~40 hrs/week

Responsibilities

The coordinator is responsible for managing IRB-approved clinical trial protocols, including patient identification, screening, and enrollment. They perform direct patient care activities and maintain strict regulatory compliance and data integrity for assigned studies.

Requirements

Candidates must have 3+ years of clinical research coordination experience and be skilled in direct patient care activities. Legal authorization to work in the US is required, as visa sponsorship is not provided.

Full job description

Description

Clinical Research Coordinator II

Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator II. The ideal candidate will possess 3+ years of clinical research coordination experience, and have a strong desire to work directly with patients.

Who We Are

ObjectiveHealth is a clinical research company that uses proprietary technology to:

  1. Increase patient access to research trials within our communities,
  2. Provide physicians with enhanced care options for current patients, and
  3. Deliver superior clinical research enrollment metrics to Pharma sponsors

All with the goal of Improving Patient Outcomes at the Point of Care. We want you to join us in doing just that.

Who You Are

  • A lover of patient interaction and skilled at providing patient care
  • A team player with a bias for action and an attitude that takes personal responsibility
  • Skilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc.
  • Skilled at performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG, etc.
  • Possess an acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set-up and maintenance, and strict protocol adherence
  • An expert communicator with the goal of fostering relationships between the research team, PIs, Sponsors, Monitors, and others
  • A strong advocate for Company values, mission, and initiatives
  • Not easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies
  • Energized by the idea of playing a role in the future of new therapy development in the areas of Gastroenterology, Urology, Dermatology, and/or Oncology

What Success Looks Like for This Role

  • Taking ownership of assigned studies and patients
  • Communicating promptly and effectively with leadership and coworkers when you have a question or see something that needs correction
  • Showing up on time, every time
  • Ensuring strict compliance to the laws, regulations, and requirements of all applicable governing bodies
  • Learning and using the technologies we provide to increase efficiency in your day-to-day activities
  • Embodying our core values of Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication

What We Offer

Competitive compensation, 401(k) with Company match, a clear career pathway for advancement within the Company, Short- and Long-Term Disability, Health Savings and Flexible Spending Accounts, Health, Dental and Vision insurance Plans, Generous PTO, Adoption Assistance, Paid Holidays, and a wide selection of other voluntary benefits.

Requirements

This job requires legal authorization to work in the US. We are not currently accepting work visas. ObjectiveHealth is an EEO Employer and an E-Verify participant.

Related keywords

Clinical ResearchIRBPatient CareGastroenterologyUrologyDermatologyOncologyeSourceAESAEPharma SponsorsRegulatory ComplianceClinical Trial ProtocolPatient Outcomes

About ObjectiveHealth

LinkedInVisit site
Industry
Research Services
Company size
201-500 employees
Headquarters
Franklin, Tennessee
LinkedIn followers
4,453
Total funding
$14M

ObjectiveHealth is a leading integrated research provider partnering with physicians and healthcare organizations to establish advanced infrastructure for research programs. The company takes an innovative approach to research that aims to improve patient outcomes at the point-of-care. Utilizing proprietary technology, processes and trained on-site personnel, ObjectiveHealth delivers significant advances in the conduct of clinical research, benefiting clients and partners while providing broader care options for patients. Approaching 31 partnered programs across 16 states and over 600 providers, ObjectiveHealth is poised for continued growth due to the realized value of their healthcare solutions for all stakeholders.

Offices: 341 Cool Springs Blvd Ste 450, Franklin, Tennessee 37067, US

Clinical ResearchGastroenterology ResearchLiver ResearchNASHFatty Liver DiseaseGI Research NetworkMetabolism ResearchCompanion DiagnosticsGI Ancillary Service ProviderPhysician Partnerships
View all jobs at ObjectiveHealth

About ObjectiveHealth

LinkedInVisit site
Industry
Research Services
Company size
201-500 employees
Headquarters
Franklin, Tennessee
LinkedIn followers
4,453
Total funding
$14M

ObjectiveHealth is a leading integrated research provider partnering with physicians and healthcare organizations to establish advanced infrastructure for research programs. The company takes an innovative approach to research that aims to improve patient outcomes at the point-of-care. Utilizing proprietary technology, processes and trained on-site personnel, ObjectiveHealth delivers significant advances in the conduct of clinical research, benefiting clients and partners while providing broader care options for patients. Approaching 31 partnered programs across 16 states and over 600 providers, ObjectiveHealth is poised for continued growth due to the realized value of their healthcare solutions for all stakeholders.

Offices: 341 Cool Springs Blvd Ste 450, Franklin, Tennessee 37067, US

Clinical ResearchGastroenterology ResearchLiver ResearchNASHFatty Liver DiseaseGI Research NetworkMetabolism ResearchCompanion DiagnosticsGI Ancillary Service ProviderPhysician Partnerships
View all jobs at ObjectiveHealth

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