11 Clinical Research Nurse Jobs in Charleston, SC
Alcanza Clinical Research is Hiring a Clinical Research Nurse Near Charleston, SC
Employment Type: Full Time
Location: Coastal Carolina Research Center | Charleston, SC
Reporting To: Nikki Shebelskie
DescriptionAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in MA, NH, MI, VA, SC, FL, GA, AL, MO, TX 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 Clinical Research Nurse works to ensure the execution of assigned studies, and performs clinical procedures, such as venipunctures, injections, prep or mixing of investigational study drugs and infusions, under the scope of the study protocol and in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.
Key ResponsibilitiesEssential Job Duties: In 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:
- 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;
- Performing procedures commensurate with licensure including vitals, ECGs/EKGs, venipunctures, injections, infusions, mixing drug and/or dispense investigational product; etc.
- 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;
- Filing SAE/Deviation reports to Sponsor and IRB as needed;
- Documenting and reporting adverse events;
- Reporting non-compliance to appropriate staff in timely manner;
- Maintaining positive and effective communication with clients and team members;
- Always practicing ALCOAC principles with all documentation;
- Be thoroughly familiar with the protocol, case report form, informed consent, source documentation, patient diary (when applicable), and study medication(s) for the assigned research study;
- 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;
- May set up, train and maintain all technology needed for studies.
- May assist with study recruitment, patient enrollment, and tracking as needed;
- Maintaining confidentiality of patients, customers and company information, and;
- Performing all other duties as requested or assigned.
Required Skills
- Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40 wpm);
- Proficiency with performing clinical procedures such as injections, vitals, EKGs, phlebotomy, infusions, etc. is required.
- 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.
- 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.
Job Summary
Full Time
$79k-98k (estimate)
05/18/2024
09/22/2024
The job skills required for Clinical Research Nurse include Accountability, Clinical Research, Confidentiality, Effective Communication, Collaboration, Scheduling, etc. Having related job skills and expertise will give you an advantage when applying to be a Clinical Research Nurse. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Clinical Research Nurse. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Clinical Research Nurse positions, which can be used as a reference in future career path planning. As a Clinical Research Nurse, it can be promoted into senior positions as a Clinical Research Associate I that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Research Nurse. You can explore the career advancement for a Clinical Research Nurse below and select your interested title to get hiring information.
If you are interested in becoming a Clinical Research Nurse, you need to understand the job requirements and the detailed related responsibilities. Of course, a good educational background and an applicable major will also help in job hunting. Below are some tips on how to become a Clinical Research Nurse for your reference.
Step 1: Understand the job description and responsibilities of an Accountant.
Quotes from people on Clinical Research Nurse job description and responsibilities
Once patients are enrolled to a trial, the research nurse may be responsible for randomization, and for collecting and recording data.
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Clinical research nurses often lead a research team to complete a trial.
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A research nurse works as a part of a research team to evaluate healthcare products and technology.
04/10/2022: Pierre, SD
Research nurses analyze data to observe trends, make predictions and reach scientific conclusions.
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Research nurses communicate regularly with patients and research team members.
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Step 2: Knowing the best tips for becoming an Accountant can help you explore the needs of the position and prepare for the job-related knowledge well ahead of time.
Career tips from people on Clinical Research Nurse jobs
Keep reading to learn all about how to become a clinical trials research nurse.
04/06/2022: Fargo, ND
Gain clinical research experience.
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Gain Experience as a Licensed Registered Nurse.
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Pass the Nurse Researcher Certification exam.
04/04/2022: Modesto, CA
There are a specific set of skills that a research nurse needs.
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Step 3: View the best colleges and universities for Clinical Research Nurse.
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