Clinical Research Coordinator
2 weeks ago
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 Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes & procedures, and in compliance with FDA, GCP, and ICH regulations and guidelines. The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs.
Key ResponsibilitiesIn collaboration with other members of the clinical research site team works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:
Under the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes & procedures, and in compliance with FDA, GCP, ICH regulations and guidelines:
- Screening of patients for study enrollment;
- Patient consents;
- Patient follow-up visits;
- Documenting in source clinic charts;
- Entering data in EDC and answers queries;
- Obtaining vital signs and ECGs;
- May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;
- Requesting and tracking medical record requests;
- Updating and maintaining logs, chart filings;
- Maintaining & ordering study specific supplies;
- Scheduling subjects for study visits and conducts appointment reminders;
- Building/updating source as needed;
- Conducting monitoring visits and resolves issues as needed in a timely manner;
- Ensuring study related reports and patient results are reviewed by investigator in a timely manner;
members;o Always practicing ALCOAC principles with all documentation;
- Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;
- Prepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;
- Handles all IRB functions for assigned studies independently, and/or with assigned regulatory team member, as needed;
- Assist with training of new research assistants and coordinators;
- Assist with scheduling and planning for visit capacity for assigned studies;
- May set up, train and maintain all technology needed for studies;
- May assist with study recruitment, patient enrollment, and tracking as needed;
- May handle more complex study assignments and volumes;
- May participate in community outreach / education events;
- Maintaining confidentiality of patients, customers and company information, and;
- Performing all other duties as requested or assigned.
Skills, Knowledge and ExpertiseMinimum Qualifications: A Medical Assistant diploma, LPN/LVN, EMT credential AND 1+ years of clinical research coordination experience, OR an equivalent combination of education and experience, is required. Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred. CCRC or CCRP credential and BLS certification preferred. Bi-lingual (English / Spanish) proficiency is required.
Required Skills:
- Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);
- Performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc
- Strong organizational skills and attention to detail.
- Well-developed written and verbal communication skills.
- Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
- Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
- Must be professional, respectful of others, self-motivated, and have a strong work ethic.
- Must possess a high degree of integrity and dependability.
- Ability to work under minimal supervision, 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.
-
Unblinded Clinical Research Coordinator I
1 month ago
Jersey City, United States DM Clinical Research Full timeJob DescriptionJob DescriptionUnblinded Clinical Research Coordinator IDM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.Duties & Responsibilities:Compound and dispense prescribed IP. ...
-
Clinical Research Coordinator III
2 months ago
Jersey City, United States DM Clinical Research Full timeJob DescriptionJob DescriptionClinical Research Coordinator IIIA CRC III will 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. To ensure study enrollment meets or exceeds Sponsors' expectations. To...
-
Clinical Research Coordinator III
7 days ago
Jersey City, United States DM Clinical Research Full timeJob DescriptionJob DescriptionClinical Research Coordinator IIIA CRC III will 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. To ensure study enrollment meets or exceeds Sponsors' expectations. To...
-
Lead Clinical Research Specialist
1 week ago
Kansas City, Missouri, United States Everest Clinical Research Services Inc Full timeCompany Overview: Everest Clinical Research Services Inc. is a premier contract research organization (CRO) delivering a comprehensive suite of expertise-driven clinical research solutions to global pharmaceutical, biotechnology, and medical device sectors. We collaborate with some of the most recognized companies and engage with numerous advanced...
-
Lead Clinical Research Specialist
1 week ago
Kansas City, Missouri, United States Everest Clinical Research Services Inc Full timeCompany Overview: Everest Clinical Research Services Inc. is a premier contract research organization (CRO) dedicated to delivering a comprehensive suite of expertise-driven clinical research solutions to global pharmaceutical, biotechnology, and medical device sectors. We collaborate with some of the most renowned companies and are involved with many of...
-
Senior Clinical Research Associate
2 months ago
Kansas City, United States Everest Clinical Research Services Inc Full timeEverest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical...
-
Lead Clinical Research Specialist
5 days ago
Kansas City, Missouri, United States Everest Clinical Research Services Inc Full timeCompany Overview: Everest Clinical Research Services Inc. is a comprehensive contract research organization (CRO) offering a wide array of expertise-driven clinical research solutions to global pharmaceutical, biotechnology, and medical device sectors. We collaborate with some of the most reputable companies and engage with many of the most innovative...
-
Clinical Research Coordinator
3 weeks ago
Lake City, United States Wake Research Full timeJob DescriptionJob DescriptionCompany DescriptionM3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). With close to 30 owned and managed research sites across the...
-
Clinical Research Coordinator
1 week ago
Oklahoma City, Oklahoma, United States Tekton Research Full timeTekton Research is in search of an Unblinded Clinical Research Coordinator to enhance our operations.This role is on-site and will involve executing Unblinded CRC responsibilities across our pharmacies.Key Responsibilities:The Unblinded Clinical Research Coordinator will primarily assist the Lead Unblinded/Pharmacy personnel in managing Investigational...
-
Clinical Research Coordinator
2 weeks ago
Oklahoma City, Oklahoma, United States Tekton Research Full timeTekton Research is currently looking for an Unblinded Clinical Research Coordinator to enhance our operations.This role is an on-site position that will involve performing Unblinded CRC responsibilities across multiple locations.Key Responsibilities:The primary function of the Unblinded Clinical Research Coordinator is to assist the Lead Unblinded/Pharmacy...
-
Clinical Research Lab Coordinator
2 days ago
Oklahoma City, Oklahoma, United States Tekton Research Full timeTekton Research is seeking a highly skilled Clinical Research Lab Coordinator to support the conduct of research in carrying out lab requirements of each study protocol.The ideal candidate will have excellent phlebotomy skills and experience with lab processing, as well as a strong understanding of clinical research principles.Key Responsibilities:Order and...
-
Lead Clinical Researcher
5 days ago
Jersey City, New Jersey, United States DM Clinical Research Full timeJob OverviewLead Clinical Researcher (MD/DO)The Lead Clinical Researcher will oversee all clinical trials in alignment with ICH, GCP, local regulations, study protocols, and organizational procedures.Key ResponsibilitiesGuarantees the medical safety and well-being of study participants through the diligent execution of clinical trials.Supports the...
-
Lead Clinical Researcher
5 days ago
Jersey City, New Jersey, United States DM Clinical Research Full timeJob OverviewLead Clinical Researcher (MD/DO)The Lead Clinical Researcher will oversee all clinical trials in accordance with ICH, GCP, local regulations, study protocols, and organizational procedures.Key ResponsibilitiesGuarantees the medical welfare and safety of participants through the careful execution and management of studies.Assists in ensuring...
-
Clinical Research Coordinator
1 month ago
Kansas City, United States Medix™ Full timeWe are looking for a self-starter to join our team in Kansas City, MO as a Clinical Research Coordinator. If you're a Clinical Research professional ready to take the next step in their career and passionate about immunology trials, apply today!We have openings for multiple CRCs in the area, so in addition to Kansas City, we are hiring a CRC at each...
-
Clinical Research Coordinator
2 months ago
West Valley City, United States START Center for Cancer Research Full timeJob DescriptionJob DescriptionThe START Center for Cancer Research (“START”) is the world’s largest global phase I oncology clinical trial research site network. Over its 17-year history, START has provided hope to cancer patients in community practices and hospitals by offering access to cutting edge early phase oncology trials throughout the US and...
-
Lead Clinical Research Investigator
5 days ago
Jersey City, New Jersey, United States DM Clinical Research Full timeJob OverviewPosition: Principal Investigator (MD/DO)The Principal Investigator will oversee all clinical trials in accordance with ICH, GCP, local regulations, study protocols, and organizational procedures.Key ResponsibilitiesSafeguards the medical well-being and safety of study participants through the diligent execution of clinical trials.Maintains...
-
Clinical Research Coordinator- 233537
7 days ago
Kansas City, United States Medix™ Full timePosition Overview:In this role you will ensure IRB approved protocols are implemented and followed; execute theinformed consent process and monitor patient status and safety; collect and organize researchdata; schedule and conduct study-specific training and site in-services to study related staff onnew or amended protocols, and educate patients and their...
-
Clinical Research Coordinator- 233537
3 days ago
Kansas City, United States Medix™ Full timePosition Overview:In this role you will ensure IRB approved protocols are implemented and followed; execute theinformed consent process and monitor patient status and safety; collect and organize researchdata; schedule and conduct study-specific training and site in-services to study related staff onnew or amended protocols, and educate patients and their...
-
Senior Clinical Research Coordinator
3 months ago
Kansas City, United States US Tech Solutions Full timeJob Description: The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials. Working in collaboration with the Principal Investigator, the Sr. CRC is...
-
Clinical Nurse Coordinator MedSurg
3 days ago
Kansas City, United States Research Medical Center Full timeDescription IntroductionDo you have the career opportunities as a(an) Clinical Nurse Coordinator MedSurg you want with your current employer? We have an exciting opportunity for you to join Research Medical Center which is part of the nation's leading provider of healthcare services, HCA Healthcare.BenefitsResearch Medical Center, offers a total rewards...