FSP Clinical Trial Coordinator I
Posted 13 days ago
You'll complete your application on Thermo Fisher Scientific's career site.
About the Role
As a Clinical Trial Coordinator I, you will become part of an international group focused on assisting with intricate clinical research programs. Your primary function involves the vital orchestration and supervision of study tasks, making sure that every action adheres to assigned matrices, quality benchmarks, and financial constraints. You will operate in a cooperative setting where you help deliver impactful medical treatments by handling project records, digital databases, and key stakeholder correspondence. This opening provides a chance to build a core understanding of clinical trial administration in a remote, highly organized pharmaceutical services workplace.
Requirements
- You should possess at least a high or secondary school diploma, though a Bachelor's degree is preferred, plus no more than one year of related experience.
- You must exhibit high levels of organization, precise attention to detail, and the capacity to function well on your own or as part of a group.
- You are required to be proficient in MS Office tools and have an aptitude for learning sophisticated clinical database software.
- Excellent command of English and pertinent local languages in both written and spoken forms is necessary, as is the capability to understand and implement regional laws and ICH Good Clinical Practices.
- You should demonstrate good decision-making, strong negotiation skills, and the adaptability to handle changing tasks in an environment with high momentum.
Responsibilities
- You will manage and record study operations, which includes performing internal and site file audits to guarantee adherence to protocols.
- Your main tasks include utilizing systems such as Activate and eTMF, handling paperwork, and reviewing study data to uphold project accuracy.
- You will facilitate the organization of investigator site records, handle trial materials, and aid in compiling materials for regulatory reviews.
- You will engage directly with research sites to secure necessary files, monitor site engagement, and record interactions as they occur.
- A major element of this role includes tracking trial milestones, reporting any compliance breaches to leadership, and offering regional insights to support site identification and feasibility evaluations.
Benefits & Perks
- This role is completely remote and allows for flexibility throughout a typical Monday-to-Friday work week.
Note: This listing is summarized and paraphrased by WorkNow from a publicly posted role. For the original wording and full details, please refer to the employer's official posting.
Similar Jobs
Inpatient Coding Supervisor – Mid-Shift
Med-Metrix
This leadership position is centered on leading and refining the output of an inpatient coding group. In this virtual capacity, you will handle daily functions to guarantee that output and precision goals are hit on a regular basis. You will act as a primary point of contact, handling task lists, verifying that Service Level Agreements are respected, and assigning tasks based on coder availability and account urgency. By building a supportive setting, you will be instrumental in upholding superior performance standards and assisting with the career growth of your personnel. Furthermore, you will focus on increasing efficiency and ensuring regulatory adherence within the unit. Your duties involve tracking performance indicators, performing routine evaluations, and working alongside quality control groups to resolve error patterns and launch correction methods. You will also participate in workflow enhancements, assist with automation programs, and ensure your staff stays current with changing coding mandates. Using analytical findings and consistent communication with management and client partners, you will guarantee that every inpatient coding task is performed with accuracy, honesty, and a dedication to excellence.
Senior Manager – Regional Head, Regulatory APAC
Cencora
In this Senior Manager and Regional Head position for Regulatory APAC, you are responsible for offering high-level regulatory guidance and directing complex international, regional, and domestic initiatives. You play a central role in ensuring premium service delivery that supports the organization’s commercial goals. Your mandate includes overseeing regulatory workflows to secure and preserve marketing approvals for a broad portfolio, covering human and animal drugs, medical equipment, beauty products, nutritional supplements, and botanical items. You are also tasked with advancing regional expansion by managing client growth, handling proposals, and pursuing business development. Additionally, you will participate in defining the practice's long-term aims, while seeking ways to enhance innovation, streamline operations, and broaden service offerings. By cultivating teamwork, you will maintain functional excellence, manage staffing requirements, and serve as a primary consultant regarding team potential and scalability within the worldwide enterprise.
Senior Art Director
Construct Digital
This agency focuses on building data-backed brand stories that produce tangible commercial success. Through a mix of artistic flair and sophisticated technical solutions, the firm drives growth in sales, lead acquisition, and ROI. The service offering includes data analysis, UX design, content marketing, and modern AI integration to optimize engagement and performance. As a Senior Art Director, you will work alongside creative technologists, planners, and strategists to deliver impactful solutions for clients throughout the Asia-Pacific territory. This pivotal position requires a blend of aesthetic leadership, hands-on production, and strategic guidance within an environment that promotes experimentation and continuous workflow improvement.