Sr. Clinical Trial Coordinator - FSP Client Dedicated

Work Schedule

Environmental Conditions

Job Description

Join Us as a Senior Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our global team, you’ll have the opportunity to provide administrative and technical support to the Project Team. As a Senior Clinical Trial Coordinator, you'll coordinate and facilitate project activities and may serve as a study lead, acting as a cross-functional liaison for the project team. You will act as a buddy during the onboarding phase and provide training to new staff as needed. Additionally, you will support departmental and cross-functional initiatives for process improvements and enhancements.

What You’ll Do:

• According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix.
  • Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system.
  • Ensures allocated tasks are performed on time, within budget and to a high quality standard. Proactively communicates any risks to project leads and line manager as appropriate.
  • Supports the maintenance of study specific documentation and global support with specific systems, tools and trackers including but not limited to: study team lists, tracking of project specific training requirements, system access management for organization/vendor/clients, and tracking of project level activity plans in appropriate system. Ensures (e)TMF is up to date by following file review schedules and documents findings in appropriate system.
  • Provides system support (i.e. GoBalto & eTMF).
  • Supports RBM activities.
  • Performs administrative tasks on assigned trials including but not limited to: timely processing of documents sent to Client (e)TMF as assigned, performing (e)TMF reviews, performing mass mailings and communications as needed, providing documents and reports to internal team members.
  • Supports scheduling and organization of client and/or internal meetings with completion of related meeting minutes.
  • Reviews and tracks local regulatory documents.
  • Transmits documents to client and centralized IRB/IEC.
  • Analyzes and reconciles study metrics and findings reports. Assists with clarification and resolution of findings related to site documentation.
  • Maintains vendor trackers.
  • Assists with coordination, compilation and distribution of Investigator Site File (ISF) and Pharmacy binder materials and non-clinical study supplies to sites.
  • Assists with study-specific translation materials and translation QC upon request.
  • May attend Kick off meeting and take notes when required.
  
  Education and Experience Requirements:
  • High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification.
  • Bachelor's degree preferred with education in medical or biological sciences or discipline associated with clinical research preferred
  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 4 years).
  In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
  
  Knowledge, Skills and Abilities:
  • Ability to work in a team or independently as required
  • Strong organizational skills and attention to detail, with proven ability to handle multiple tasks efficiently and effectively
  • Proven ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency
  • Strong customer focus
  • Demonstrated flexibility and adaptability to reprioritize workload and provide efficient support to meet changing project timelines
  • Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and closeout
  • Excellent English language and grammar skills and proficient local language skills as needed
  • Good presentation skills
  • Excellent computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems
  • Ability to successfully complete PPD clinical training program
  • Self-motivated, positive attitude with effective strong interpersonal skills
  
  
  
  Working Conditions and Environment:
  • Work is performed in an office/ laboratory/clinical/ and/or home office environment with exposure to electrical office equipment.
  • Occasional drives to site locations. Potential Occasional travel required