Clinical Research Coordinator Job at Eximia Research, Murfreesboro, TN

MnRrK2pidFNqV254Uk9wdGx2R0dkRDArM0E9PQ==
  • Eximia Research
  • Murfreesboro, TN

Job Description

Company Description

Eximia Research is a fully Integrated research sites network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). Our premier, multidisciplinary wholly owned research sites located across country and known for excellent trial execution, rapid subject recruitment/enrollment and delivery of a quality data.

Clinical Research Coordinator

Eximia Clinical Research is looking for a CRC to join our team. As the CRC, you will act as a member of the clinical trial team to conduct and manage clinical trial(s) from start up through study close out in accordance with the study protocol, GCP, and Eximia Clinical Research’s SOPs.

Role & Responsibilities:

  • Serve as member of a study team to execute clinical trials
  • Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Eximia Clinical Research’s SOPs
  • Implement and coordinate assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports.
  • Apply project management concepts to manage risk and improve quality in the conduct of a clinical research study
  • Develop, coordinate, and implement research and administrative strategies to successfully manage assigned protocols.
  • Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors.
  • Ensure good documentation practices are applied by team members when collecting and correcting data, transferring data to sponsor/CRO data capture systems and resolving queries
  • Ensure confidentiality of patient protected health information, sponsor confidential information and Eximia Clinical Research confidential information is maintained by all team members
  • Develop communication and escalation strategies within teams to that ensure patient safety is upheld and all adverse events, serious adverse events, and adverse events of special interest are followed and reported in accordance with the protocol and Eximia Clinical Research SOPs
  • Ensure all data is entered into the sponsor's data portal and all queries are resolved in a timely manner
  • Ensure staff are delegated and trained appropriately and documented
  • Ensure the creation, collection and submission of regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations and IRB requirements.
  • Evaluate potential subjects for participation in clinical trials including phone and in person prescreens.
  • Create and execute recruitment strategies in conjunction with patient recruitment staff
  • Incorporate key timelines, endpoints, required vendors, and patient population when planning for each assigned protocol.
  • Incorporate understanding of how decisions affect the bottom-line including links between operations and company’s financial performance and how it is essential to create value of all stakeholders of the organization when planning for each assigned protocol.
  • Incorporate understanding of product development lifecycle and significance of protocol design including critical data points when planning for each assigned protocol
  • Develop Quality Control strategies for team member projects
  • Perform clinical duties (e.g. Drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing) within scope
  • Promote respect for cultural diversity and conventions with all individuals.
  • Understand the disease process or condition under study
  • Other duties as assigned

Qualifications

Education/Experience:

  • Bachelor’s degree and 2 years as a Clinical Research Coordinator

Required Licenses/Certifications:

  • Phlebotomy if applicable and required by state law
  • Intravenous/Intramuscular dose administration and preparation if applicable and required by state law
  • Certified Clinical Research Coordinator through ACRP or SOCRA within six months of being in the role

Required Skills:

  • Advanced knowledge of medical terminology
  • Proficient in the use of the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone.
  • Proficient ability to work in a fast-paced environment
  • Advanced verbal, written, and organizational skills
  • Advanced interpersonal and communication skills
  • Advanced ability to work as a team player
  • Advanced ability to read, write, and speak English
  • Demonstrated ability to multi-task
  • Advanced ability to follow written guidelines
  • Demonstrated ability to work independently, plan and prioritize multiple deliverables and objectives
  • Demonstrated ability to be flexible/adapt as daily schedule may change rapidly
  • Must be detail oriented
  • Proficient problem solving and strategic decision making ability.
  • Advanced in accepting individual responsibility for actions taken and demonstrating professionalism when judged, critiqued and/or praised.
  • Proficient leader, mentor and team builder

Job Tags

Flexible hours,

Similar Jobs

Research Institute of Orlando

Clinical Research Coordinator Job at Research Institute of Orlando

 ...Company Description Research Institute of Orlando (RIO), LLC specializes in FDA-regulated clinical research trials. We focus on Neurology and Healthy patient trials from around the world. Our mission is to facilitate the development of regulated medications through... 

China Global Connections

Physics Teacher Job at China Global Connections

We are looking for a Physics Teacher for an InternationalSchool based in Beijings Chaoyang district. This is a full-time positionstarting in August 2025. About the schoolInternational school based in Beijings Chaoyang area andone of the leading providers of K12 education... 

Allen, Glaessner, Hazelwood & Werth, LLP

Litigation Attorney Job at Allen, Glaessner, Hazelwood & Werth, LLP

 ...applicants will be considered for a fast track to partnership.We will also consider experienced applicants who are interested in part time or contract work. Salary is negotiable depending on experience. To apply, please submit a cover letter, resume, and writing sample... 

Catholic Charities Diocese of Charlotte

Volunteer Coordinator Job at Catholic Charities Diocese of Charlotte

 ...you passionate about service and building community? Catholic Charities Diocese of Charlotte is seeking a dedicated and organized Volunteer Coordinator to lead our volunteer program and strengthen our mission of service.In this dynamic role, you will:Recruit, train,... 

Pacific Coast Speech Services

Speech Language Pathologist Job at Pacific Coast Speech Services

 ...interdisciplinary team members to ensure educational benefit. Consultation & Instruction : Consult with team members, including families, to maximize generalization of target skill sets. May oversee and support the Speech Language Pathologist Assistant (SLPA),...