FCN MEDICAL GROUP
 

Job Description: Clinical Research Coordinator

 

We are seeking a detail-oriented and organized Clinical Research Coordinator (CRC) to join our research team. The CRC will play a pivotal role in managing and facilitating clinical trials from inception to completion, ensuring compliance with regulatory requirements and study protocols. This position requires a strong understanding of clinical research processes and excellent communication skills to liaise with patients, investigators, and research staff.

 

The Clinical Research Coordinator will be responsible for overseeing the day-to-day operations of clinical studies, including participant recruitment, informed consent procedures, and scheduling study visits. The coordinator will maintain accurate and timely documentation of study data, ensuring adherence to Good Clinical Practice (GCP) guidelines and institutional policies. Additionally, the CRC will collaborate with principal investigators to prepare and submit regulatory documents to institutional review boards (IRBs) and funding agencies, as well as tracking adverse events and reporting findings. The role requires meticulous attention to detail, problem-solving skills, and a commitment to maintaining the integrity of the research process while fostering a supportive environment for study participants.

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Job Description: Clinical Research Associate

 

We are looking for a dedicated and detail-oriented Clinical Research Associate (CRA) to join our dynamic research team. The CRA will be instrumental in monitoring and managing clinical trials to ensure compliance with regulatory requirements and adherence to study protocols. This position requires a strong understanding of clinical research methodologies, excellent communication skills, and the ability to work collaboratively with various stakeholders, including investigators, site staff, and regulatory agencies.

 

As a Clinical Research Associate, your primary responsibilities will include conducting site visits to assess trial progress, evaluating the collection and accuracy of study data, and ensuring that trial sites comply with Good Clinical Practice (GCP) guidelines. You will be responsible for reviewing and verifying the integrity of study documentation, resolving any discrepancies, and providing training and guidance to site personnel as needed. Additionally, the CRA will assist in the development and management of study timelines, facilitate communication between the study team and the site, and prepare detailed reports and presentations summarizing findings and recommendations. The ideal candidate will possess strong organizational skills, a proactive approach to problem-solving, and the ability to manage multiple projects simultaneously while adhering to deadlines.

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Job Description: Clinical Site Manager

 

We are seeking an experienced and proactive Clinical Site Manager (CSM) to oversee and coordinate the operational aspects of clinical trials at our research sites. The CSM will play a critical role in ensuring the successful execution of clinical studies while maintaining compliance with regulatory requirements, study protocols, and Good Clinical Practice (GCP) guidelines. This position requires a solid understanding of clinical research processes, strong leadership abilities, and excellent communication skills to effectively manage site staff and foster relationships with key stakeholders.

 

As a Clinical Site Manager, your responsibilities will include managing day-to-day site operations, ensuring that studies are conducted according to protocol specifications and within timelines and budgets. You will oversee staff training, monitor recruitment strategies, and ensure that patients are selected and enrolled according to the study's inclusion and exclusion criteria. The CSM will also be responsible for maintaining accurate and complete documentation of site activities, including study records, regulatory files, and source data verification, ensuring readiness for audits and inspections. Collaboration with cross-functional teams, including clinical research associates, principal investigators, and institutional review boards (IRBs), will be key to facilitating smooth communication and problem resolution throughout the study lifecycle.

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Job Description: Clinical Research Project Manager

 

We are seeking a highly motivated and experienced Clinical Research Project Manager (CRPM) to lead and manage clinical trials from conception through to completion. The CRPM will be responsible for the overall planning, execution, and oversight of clinical research projects, ensuring that they are delivered on time, within scope, and in compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. The ideal candidate will possess strong leadership skills, exceptional organizational capabilities, and a deep understanding of clinical research processes.

 

In this role, the Clinical Research Project Manager will oversee the development of project plans, including timelines, budgets, and resource allocation. You will be responsible for coordinating cross-functional teams, including clinical research associates, site managers, and data management personnel, to ensure effective collaboration throughout the project lifecycle. The CRPM will also be tasked with facilitating communication between internal stakeholders and external partners, including investigational sites and regulatory authorities. Key responsibilities include monitoring project progress, identifying and mitigating risks, and ensuring adherence to quality standards. Moreover, the CRPM will prepare and present project updates to senior management and stakeholders, ensuring transparency and alignment with organizational goals.