Clinical Research Manager jobs in South Carolina
Clinical Research Manager manages the clinical monitoring process and the administration of clinical trials. Supervises CRAs in in-house and on-site monitoring, filing, and clinical trial administration. Being a Clinical Research Manager oversees adherence to SOPs, Good Clinical Practice and FDA regulations. Helps with the development and implementation of clinical processes, procedures, and programs. Additionally, Clinical Research Manager may require a master's degree in nursing. May require ACRP or SOCRA Clinical Research Professional exam completion. Typically reports to a director. The Clinical Research Manager manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. To be a Clinical Research Manager typically requires 5 years experience in the related area as an individual contributor. 1-3 years supervisory experience may be required. Extensive knowledge of the function and department processes. (Copyright 2024 Salary.com)
Recently Added Clinical Research Manager jobs
Clinical Research Nurse
- Alcanza Clinical Research
-
Charleston, SC
FULL_TIME
-
Department: Operations
Employment Type: Full Time
Location: Coastal Carolina Research Center | Charleston, SC
Reporting To: Nikki Shebelskie
Description
Alcanza 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 Responsibilities
Essential 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: - 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;
- 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.
- 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.
- 6 Days Ago
Minimum Qualifications: A Bachelor's degree in Nursing (BSN) AND a minimum of 1 year of clinical experience, OR an equivalent combination of education and experience, is required. An active, unrestricted RN license, in state of work location, is required. BLS certification required. Bi-lingual (English / Spanish) proficiency is a plus.
Required Skills
Medical Assistant / Clinical Research Assistant
- Alcanza Clinical Research
-
Charleston, SC
FULL_TIME
- Medical Assistant / Clinical Research Assistant Department: Operations Employment Type: Full TimeLocation: Coastal Carolina Research Center | Charleston, SCReporting To: Nikki ShebelskieDescriptionAlc...
- 24 Days Ago
Clinical Research Nurse
- Medical Research Network
-
Charleston, SC
PART_TIME
- Per Diem RN - Clinical Trials (performed in-home) Calling all Infusion, Emergency, and Clinical Research Registered Nurses!! Are you looking to expand your skillset? Would you like to help to bring li...
- Just Posted
Clinical Research Manager
- Charleston ENT & Allergy
-
Charleston, SC
FULL_TIME
- We are an eclectic team inspired by intellectual curiosity and a passion for exceptional patient care. Here we lead with compassion, direction, and focus. As a Clinical Research Manager, we define suc...
- 19 Days Ago
Territory Business Manager
- iS CLINICAL
-
Charleston, SC
FULL_TIME
- The Territory Business Manager will be responsible for territory sales development and management. Have the ability to follow corporate direction, management direction and to execute brands identity i...
- 1 Day Ago
Principal Investigator
- Velocity Clinical Research, Inc.
-
Anderson, SC
FULL_TIME
- Overview Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we ...
- 3 Days Ago
Clinical Research Manager jobs at Popular Companies
Clinical Research Manager
- Colgate-Palmolive
-
Piscataway, NJ
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Clinical Research Manager
- Alphatec Spine
-
Carlsbad, CA
- An ATEC Clinical Research Manager (CRM) supports the company's Clinical Research initiatives by managing the clinical re...
- 6/11/2024 12:00:00 AM
Clinical Research Manager
- Texas Oncology
-
Austin, TX
- Overview: Texas Oncology is looking for a full-time Clinical Research Manager to join our team! This position will suppo...
- 6/9/2024 12:00:00 AM
Clinical Research Manager
- Triton Medical Robotics
-
Burlingame, CA
- Triton Medical Robotics, a division of Neptune Medical, is an innovative, venture capital funded medical device startup ...
- 6/9/2024 12:00:00 AM
Clinical Research Manager
- Charleston ENT & Allergy
-
Charleston, WV
- We are an eclectic team inspired by intellectual curiosity and a passion for exceptional patient care. Here we lead with...
- 6/9/2024 12:00:00 AM
Clinical Research Manager
- SQRL
-
Winter Park, FL
- Highlights $70,000 - $80,000 salary + up to 10% bonus! Full Benefits and Consistent M-F schedule Fast growing company wi...
- 6/8/2024 12:00:00 AM
Clinical Research Manager
- SQRL
-
San Antonio, TX
- Highlights $75,000 - $80,000 salary Full benefits including: Health, Dental, Vision, 15 days PTO, and 401k with 4%match ...
- 6/7/2024 12:00:00 AM
Clinical Research Manager
- Houston Journal of Health Law & Policy
-
Houston, TX
- Description Oversees investigator-initiated and sponsored clinical research projects. Manages graduate students, post-do...
- 6/7/2024 12:00:00 AM
About South Carolina
South Carolina (/ˌkærəˈlaɪnə/ (listen)) is a state in the Southeastern United States and the easternmost of the Deep South. It is bordered to the north by North Carolina, to the southeast by the Atlantic Ocean, and to the southwest by Georgia across the Savannah River.
South Carolina became the eighth state to ratify the U.S. Constitution on May 23, 1788. South Carolina became the first state to vote in favor of secession from the Union on December 20, 1860. After the American Civil War, it was readmitted into the United States on June 25, 1868.
South Carolina is the 40th most extensive and 23...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Manager jobs
$94,160 to $124,748
Most Popular Cities in South Carolina for Clinical Research Manager Jobs
What does a Clinical Research Manager do?
Clinical Research Manager in Richland, WA
Clinical research managers must plan every phase of research programs, from initial concept through product development and clinical trials to submission for approval by the U.S.
November 27, 2019
Clinical Research Manager in Spartanburg, SC
Research is both the foundation and the future of medicine.
December 17, 2019
Clinical Research Manager in Vallejo, CA
When transitioning into the clinical research field from a science background, it is good to know what experience you have, what positions you are interested in, and what careers are most appropriate for your background.
December 19, 2019