Phoenix, Arizona, United States · On-site
$100k–$120k/yr
Job DetailsJob Location: Phoenix - Phoenix, AZ 85012Salary Range: $100,000.00 - $120,000.00 Salary/yearThe Site Manager's job is to ensure that quality research is conducted at assigned investigative sites in accordance …
Skills: Clinical Research Coordination, Staff Management, FDA Regulations, ICH-GCP Guidelines, Patient Consent
San Antonio, Texas, United States · On-site
Job DetailsJob Location: San Antonio, TX - San Antonio, TX 78207The Clinical Research Coordinator I will work at site to help ensure that quality research is conducted at the assigned investigative sites in accordance wi…
Skills: Clinical Research Coordination, Patient Recruitment, Informed Consent, Data Entry, Query Resolution
San Antonio, Texas, United States · On-site
Job DetailsJob Location: San Antonio, TX - San Antonio, TX 78207The Enrollment Coordinator is responsible for educating patients and potential patients on the company and the studies we are enrolling for with the goal of…
Skills: Patient Education, Patient Enrollment, Customer Service, Sales, Bilingual Spanish
Albuquerque, New Mexico, United States · On-site
Job DetailsJob Location: Albuquerque , NM - Albuquerque, NM 87106DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator I to join our team. This individual will be responsible for dispensing I…
Skills: Investigational Product Management, Clinical Data Auditing, Regulatory Documentation, Drug Dosing, IP Accountability
Karachi Division, Sindh, Pakistan · On-site
Job DetailsJob Location: Corporate - Karachi (KHI) - Karachi, Sindh 75600The Administrative Assistant will administratively support the Site Development & Integration team projects by performing day-to-day tasks involvin…
Skills: Organizational Skills, Verbal Communication, Written Communication, Time Management, Computer Skills
New York, New York, United States · On-site
$24/hr–$28/hr
Job DetailsJob Location: Brooklyn, NY (AOM) - Brooklyn, NY 11220Salary Range: $24.00 - $28.00 HourlyThe Research Assistant II (Non lab) will be responsible for assisting the clinical research staff in conducting clinical…
Skills: Clinical Research, Patient Data Collection, Phlebotomy, Medical Terminology, EKG/ECG
Houston, Texas, United States · On-site
$80k–$96k/yr
Job DetailsJob Location: CyFair - Houston, TX 77065Salary Range: $80,000.00 - $96,000.00 Salary/yearA Study Manager is responsible to ensure that quality research is conducted at assigned investigative sites in accordanc…
Skills: Clinical Research Management, ICH-GCP Guidelines, FDA Regulations, Patient Consent, Data Quality Management
Houston, Texas, United States · On-site
Job DetailsJob Location: CyFair - Houston, TX 77065The Clinical Research Coordinator III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulat…
Skills: Clinical Research Coordination, ICH-GCP Guidelines, FDA Regulations, Patient Consent, Data Entry
Philadelphia, Pennsylvania, United States · On-site
$100k–$120k/yr
Job DetailsJob Location: Philadelphia - Philadelphia, PA 19107Salary Range: $100,000.00 - $120,000.00 Salary/yearThe Site Manager's job is to ensure that quality research is conducted at assigned investigative sites in a…
Skills: Clinical Research Coordination, Site Management, FDA Regulations, ICH-GCP Guidelines, Staff Supervision
Sugar Land, Texas, United States · On-site
Job DetailsJob Location: Sugarland - Sugar Land, TX 77478The Clinical Research Coordinator III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA R…
Skills: Clinical Research Coordination, ICH-GCP Guidelines, FDA Regulations, Patient Consent, Data Entry
Hoover, Alabama, United States · On-site
$26/hr–$30/hr
Job DetailsJob Location: Boston - Brookline, MA 02446Salary Range: $26.00 - $30.00 HourlyThe Research Assistant II (Lab) will be responsible for assisting the clinical research staff in conducting clinical research trial…
Skills: Phlebotomy, Clinical Research, Patient Data Collection, EKG/ECG, Blood Pressure Monitoring
Irving, Texas, United States · On-site
Job DetailsJob Location: Dallas, TX - Irving, TX 75061The Phlebotomist (or Certified Medical Assistant) will be responsible for assisting the clinical research staff in conducting clinical research trials. DUTIES & RESPO…
Skills: Phlebotomy, Clinical Research, Patient Data Collection, Specimen Management, Medical Terminology
Tomball, Texas, United States · On-site
Job DetailsJob Location: Tomball 13406 - Tomball, TX 77375DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator I to join our team. This individual will be responsible for dispensing Investig…
Skills: Investigational Product Management, Clinical Data Auditing, Regulatory Documentation, Drug Dosing, IP Accountability
Tomball, Texas, United States · On-site
Job DetailsJob Location: Tomball 13406 - Tomball, TX 77375The Clinical Research Coordinator I will work at site to help ensure that quality research is conducted at the assigned investigative sites in accordance with the…
Skills: Clinical Research Coordination, Patient Recruitment, Informed Consent, Data Entry, Query Resolution
Philadelphia, Pennsylvania, United States · On-site
Job DetailsJob Location: Philadelphia - Philadelphia, PA 19107A Study Manager is responsible to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regul…
Skills: Clinical Research Management, ICH-GCP Guidelines, FDA Regulations, Patient Consent, Data Quality Management
Karachi Division, Sindh, Pakistan · On-site
Job DetailsJob Location: Corporate - Karachi (KHI) - Karachi, Sindh 75600Position Type: Contractor (CONT)Education Level: Bachelor's DegreeTravel Percentage: NoneJob Category: FinanceThe Investigator Financial Analyst se…
Skills: Financial Analysis, Budgeting, Forecasting, Financial Reporting, Interpersonal Communication
Irving, Texas, United States · On-site
Job DetailsJob Location: Dallas, TX - Irving, TX 75061The Clinical Research Coordinator II (Denton, TX) will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor pr…
Skills: Clinical Research Coordination, ICH-GCP Guidelines, FDA Regulations, Patient Recruitment, Data Entry
Indianapolis, Indiana, United States · On-site
Job DetailsJob Location: Indianapolis - Indianapolis, IN 46254DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator I to join our team. This individual will be responsible for dispensing Inve…
Skills: Investigational Product Management, Clinical Data Auditing, Regulatory Documentation, Drug Dosing, IP Accountability
Irving, Texas, United States · On-site
$90/hr–$130/hr
Job DetailsJob Location: Dallas, TX - Irving, TX 75061Salary Range: $90.00 - $130.00 HourlyThe Principal Investigator is accountable and responsible for ensuring adherence to protocol requirements, protecting the rights …
Skills: Clinical Research, Patient Consent, Medical Care Management, Protocol Adherence, GCP/ICH Guidelines
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The Site Manager ensures quality research is conducted at investigative sites in compliance with sponsor protocols, FDA regulations, and ICH/GCP guidelines. They are responsible for supervising site staff, managing subject enrollment, and ensuring high-quality data reporting.
Candidates should ideally hold a bachelor's or advanced degree and have at least 4 years of clinical research coordinator experience, including 2 years in management. CCRC certification and proficiency in English (and preferably Spanish) are highly desired.
Job DetailsJob Location: Phoenix - Phoenix, AZ 85012Salary Range: $100,000.00 - $120,000.00 Salary/yearThe Site Manager's job is to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. Also To ensure study enrollment meets or exceeds Sponsors' expectations and company goals are achieved on a timely basis.
Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s).
Responsible for immediate supervision and performance of the assigned site staff under the supervision of the Site Director or Director of Site Operations.
Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
Sponsor-provided and IRB-approved Protocol Training
All relevant Protocol Amendments Training
Any study-specific Manuals Training as applicable
Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
It is the responsibility of the Site Manager to make sure all the relevant training is completed prior to performing any applicable tasks on the assigned study.
Ensuring visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s) and appropriate as well as timely follow-up on the action items, at their respective sites.
Make sure that the most recent versions of the Protocol, Informed Consents, Study Manuals and all the other relevant study-related documents are utilized and implemented at all times for the assigned protocol(s) at their respective site(s).
Ensuring clinical trial management from FPFV to study close out with strict adherence to study protocol, adherence to all other relevant study manuals, study documents, ICH-GCP Guidelines, FDA Regulations, and ALCOA-C standards, organizational SOPs, and guidance documents.
Ensuring data quality, subject retention, and compliance, timely and adequate study data reporting on the assigned protocol(s) being conducted at their respective site(s).
Accomplishing site objectives by managing staff; facilitating staff training as applicable; communicating job expectations
Coaching, counseling, and disciplining the employees as applicable.
To develop, coordinate, and enforce site-specific systems, policies, procedures, and productivity standards.
Communicating and effective implementation of strategic goals from senior management to the site team.
Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
Strive to ensure weekly, monthly, and quarterly assigned goals are met for their respective site(s).
Being prepared for and available at all required company meetings.
Submitting required administrative paperwork per company timelines.
Occasionally attending out-of-town Investigator Meetings.
Conduct patient consent discussions and ensure comprehension of medical procedures, risks, benefits, and alternatives
Provide clear explanations of study protocols and ensure patients' understanding before obtaining their consent
Facilitate effective communication between patients, healthcare providers, and research staff
Any other matters as assigned by management.
Bachelor’s degree preferred
Advanced degree preferred
At least 4 years of clinical research coordinator experience, including 2 years of management experience at a clinical research organization.
Certified Clinical Research Coordinator (CCRC) or equivalent certification preferred.
Solid teamwork, organizational, interpersonal, and problem-solving skills and attention to detail.
Reading Comprehension — Understanding written sentences and paragraphs in work-related documents.
Speaking and Writing to communicate effectively as appropriate for the needs of the audience.
Ability to multitask, adhere to deadlines, and work both independently and cooperatively with interdisciplinary teams.
Strong computer skills in relevant software and related clinical systems are required.
Comprehensive knowledge of FDA regulations, ICH-Good Clinical Practices (GCP) and ISOs.
Proficient communication and comprehension skills both verbal and written in the English language are required.
Proficient Bi-lingual (English/Spanish) communication and comprehension skills both in verbal and written are preferred.
Qualifications
20 years of innovation in medical research. Excellence in Patient Centricity.
DM Clinical Research is a network of clinical trial investigator sites with headquarters based out of Houston, Texas. We are the link connecting pharmaceutical and research organizations to caring individuals seeking to power the advancement of medicine. We work with qualified physicians with a diverse range of specialties—including cardiology, endocrinology, pediatrics, rheumatology, pulmonology and family medicine—and have conducted a wide variety of studies with successful enrollment targets. Websites: http://www.dmclinical.com
Offices: 6550 Mapleridge, Suite 201, Houston, TX 77801, US · 13406 Medical Complex Dr, Tomball, Texas 77375, US · 20180 W. 12 Mile Rd, Ste 400, Southfield, MI 48076, US · 231 N Broad St., 3rd Floor, Philadelphia, PA 19107, US · 2021 N MacArthur Blvd, Irving, Texas 75061, US
20 years of innovation in medical research. Excellence in Patient Centricity.
DM Clinical Research is a network of clinical trial investigator sites with headquarters based out of Houston, Texas. We are the link connecting pharmaceutical and research organizations to caring individuals seeking to power the advancement of medicine. We work with qualified physicians with a diverse range of specialties—including cardiology, endocrinology, pediatrics, rheumatology, pulmonology and family medicine—and have conducted a wide variety of studies with successful enrollment targets. Websites: http://www.dmclinical.com
Offices: 6550 Mapleridge, Suite 201, Houston, TX 77801, US · 13406 Medical Complex Dr, Tomball, Texas 77375, US · 20180 W. 12 Mile Rd, Ste 400, Southfield, MI 48076, US · 231 N Broad St., 3rd Floor, Philadelphia, PA 19107, US · 2021 N MacArthur Blvd, Irving, Texas 75061, US
