Clinical Research Director jobs in Summerville, SC

Clinical Research Director directs and oversees the clinical research function for a healthcare organization. Develops research studies and creates standards and guidelines for clinical research services and programs. Being a Clinical Research Director ensures adherence to standard operating procedures, good clinical practice and FDA regulations. Requires an advanced degree. Additionally, Clinical Research Director typically reports to top management. The Clinical Research Director manages a departmental sub-function within a broader departmental function. Creates functional strategies and specific objectives for the sub-function and develops budgets/policies/procedures to support the functional infrastructure. Deep knowledge of the managed sub-function and solid knowledge of the overall departmental function. To be a Clinical Research Director typically requires 5+ years of managerial experience. (Copyright 2024 Salary.com)

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Medical Assistant / Clinical Research Assistant
  • Alcanza Clinical Research
  • Charleston, SC FULL_TIME
  • Medical Assistant / Clinical Research Assistant

    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 and AL. 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 Research Assistant (RA) will perform administrative tasks as needed for the successful operation of the clinical research site.


    Key Responsibilities

    Responsibilities may include but are not limited to:
    • Assists with the basic screening of patients for study enrollment;
    • Assists with patient follow-up visits;
    • Documents in source clinic charts;
    • Enters data in EDC and answers queries;
    • Request and track medical record requests;
    • Enters data in EDC and answers queries;
    • May assist with vitals, EKGs, phlebotomy as needed;
    • Assists the CRC with updating and maintaining logs and filing in charts, and with chart filing; and
    • Schedules subjects for study visits, conducts appointment reminders, and reschedules visits if needed;
    • Ensures study-related reports and patient results are reviewed by the Research Coordinator and/or investigator in a timely manner.
    • Assists the CRC and/or Manager with study recruitment, patient enrollment, and tracking as needed;
    • Maintains strict confidentiality of patients, employees, customers, and company information at all times and adheres to HIPAA Guidelines; and
    • Perform all other duties as requested or assigned.


    Skills, Knowledge and Expertise

    Minimum Qualifications: An Associate’s degree OR a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience, is required. Bi-lingual (English / Spanish) proficiency is a plus.

    Required Skills:
    • Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40 wpm).
    • Must possess 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.
  • 1 Day Ago

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Clinical Research Assistant / Medical Assistant
  • Alcanza Clinical Research
  • Charleston, SC FULL_TIME
  • Clinical Research Assistant / Medical AssistantDepartment: Operations Employment Type: Full TimeLocation: Coastal Carolina Research Center | Charleston, SCReporting To: Nikki ShebelskieDescriptionAlca...
  • 1 Month Ago

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Patient Recruiter
  • Alcanza Clinical Research
  • Charleston, SC FULL_TIME
  • Patient Recruiter Department: Patient Recruitment Employment Type: Full TimeLocation: Coastal Carolina Research Center | Charleston, SCReporting To: Jade ClarkDescriptionAlcanza is a growing multi-sit...
  • 23 Days Ago

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DIRECTOR OF SAFETY
  • Thorne Research Inc
  • SUMMERVILLE, SC FULL_TIME
  • Director of Safety- Reports to Vice President of Human Resources. Role will include 4 direct reports including an EHS Manager, Safety Lead, and two Safety Techs. Role is 100% onsite at our manufacturi...
  • 3 Days Ago

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FACILITIES DIRECTOR
  • Thorne Research Inc
  • SUMMERVILLE, SC FULL_TIME
  • FACILITIES DIRECTOR 100% onsite in Summerville, SC. Oversight of two locations in Summerville, SC, Warehouse in Benicia CA, corporate headquarters in NY, and small location in Madison, WI. Summerville...
  • 7 Days Ago

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DIRECTOR, TAX
  • Thorne Research Inc
  • SUMMERVILLE, SC FULL_TIME
  • At Thorne we make products that matter - ones that make people's lives better. Each day begins with a mission to help others discover and achieve their best health. We count on our team members to cha...
  • 1 Month Ago

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0 Clinical Research Director jobs found in Summerville, SC area

Summerville is a town in the U.S. state of South Carolina situated mostly in Dorchester County with small portions in Berkeley and Charleston counties. It is part of the Charleston-North Charleston-Summerville Metropolitan Statistical Area. The population of Summerville at the 2010 census was 43,392, and the estimated population was 50,213 as of June 1, 2018. The center of Summerville is in southeastern Dorchester County; the town extends northeast into Berkeley and Charleston counties. It is bordered to the east by the town of Lincolnville and to the southeast by the city of North Charleston....
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Director jobs
$134,998 to $182,241
Summerville, South Carolina area prices
were up 1.5% from a year ago

Clinical Research Director in Killeen, TX
We are Looking for an Assistant Director for the Center for Clinical Research Education.
December 07, 2019
Clinical Research Director in Springfield, IL
During the Clinical Research Operations Forum a few weeks ago, Stephen Sonstein, Ph.D., Professor & Program Director for Clinical Research Administration at Eastern Michigan University spoke on the shift in clinical research going from a focus on regulatory compliance to a standardization of competencies for professionals working in the field.
February 06, 2020
Clinical Research Director in Olympia, WA
You might occasionally be able to enter from the administration side - for example, you could start as a study-site coordinator in the NHS or as a clinical trials administrator.
January 28, 2020