Clinical Trial Coordinator - London, United Kingdom - Thermo Fisher Scientific

Thermo Fisher Scientific

Verified Company

London, United Kingdom

2 weeks ago

Posted by:

Tom O´Connor

beBee Recruiter

Description

Clinical Trial Coordinator - Client dedicated, London (HYBRID)
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale.

Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer.

We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.

With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.

Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.

Location/Division Specific Information:

FSP (Functional Service Partnership) is a partnership between Thermo Fisher Scientific and our clients. In this position, employees will be sourced to work with a specific client. This position would require - 3 days in our sponsor's offer in Brentford (moving to central London in 2024)

Discover Impactful Work:

Provides administrative and technical support to the Project Team.

Supports audit readiness by ensuring files are reviewed, aids the development of site activation, and develops collaborative relationships with investigators and site personnel.

Supports training of new staff and participates in departmental initiatives to aid in process improvements/enhancements.

A day in the Life:

Coordinates, oversees and completes functions on assigned trial(s) activities.
Performs department, Internal, Country and Investigator file reviews as assigned and documents findings. Proactively communicates any risks to project leads and line manager as appropriate.
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, distributing mass mailings and communications as needed, providing documents and reports to internal team members.
Reviews and tracks local regulatory documents. Maintains vendor trackers.
Analyzes and reconciles study metrics and findings reports. Assists with clarification and resolution of findings related to site documentation.
Maintains knowledge of and understands SOPs, client SOPs/directives, and current regulatory guidelines as applicable to services provided.
Ensures that trial status information relating to activities is accurately maintained in the database and current at all times.
Trains new personnel in processes and systems.
Ensures (e)TMF is up to date by following file review schedules and documenting findings in appropriate system(s).
May support scheduling and organization of client and/or internal meetings with completion of related meeting minutes.
May assist with startup activities and support startup team in Regulatory submissions.
Works in collaboration with teammates to achieve targeted deadlines for assigned projects. Connect with the team and appropriate clinical personnel regarding site issues and risks.
May act as the local expert regarding site capacity and experience. Work with key local personnel to gather knowledge base and recommend additional sites. Harnesses this knowledge base when performing local tiering of sites.

Education:

Bachelor's degree preferred. In some cases, additional vocational qualifications may be considered in lieu of a degree.

Experience:

Previous experience that provides the knowledge, skills, and abilities to perform the job (at least 1 year). Strong experience in CTMS systems and eTMF systems.

Knowledge, Skills, Abilities:

Strong organizational skills and attention to detail, with proven track record to handle multiple tasks efficiently and effectively
Proven ability to effectively analyze projectspecific 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
Good presentation skills
Excellent digital literacy, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems
Selfmotivated, positive attitude with effective strong interpersonal skills
Effective oral and written English communication skills, with the ability to communicate effectively with medical personnel
Excellent interpersonal skills
Strong attention to detail and quality of documentation
Good digital literacy and the ability to learn appropriate software
Basic medical/therapeutic area and medical terminology knowledge
Ability to work in a team environment or independently.
Ability to attain and maintain a solid understanding of GCP and applicable SOPs
Proven flexibilit