Clinical Trial Coordinator

Work Schedule

Environmental Conditions

Job Description

At Thermo Fisher Scientific youll 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 lifechanging 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.

Our global Clinical Operations colleagues within our PPD clinical research services provide endtoend support for clinical trials from study start up to monitoring through to study close out across commercial and government contracts. Together we help clients define and develop clinical programs minimize delays and execute highquality costefficient clinical studies.

Position Overview:

As a Clinical Trial Coordinator you will provide administrative and technical support to the Project Team. You will support audit readiness by ensuring files are reviewed on schedule detailed in the organizations WPD and department guidance document.

Essential Functions:

• 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 highquality standard. Proactively communicates any risks to project leads.
• Supports the maintenance of study specific documentation and systems including but not limited to: study team lists tracking of project specific training requirements system access management and tracking of project level activity plans 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 of client and/or internal meetings.
• 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 nonclinical study supplies to sites.
• Assists with studyspecific translation materials and translation QC upon request.

Keys for Success:

Education and Experience:

• High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification.
• Bachelors degree preferred.
• Previous experience that provides the knowledge skills and abilities to perform the job (comparable to 0 to 1 year).

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 Abilities:

• Ability to work in a team or independently as required
• Good organizational skills and strong attention to detail with proven ability to handle multiple tasks efficiently and effectively
• Demonstrated ability to effectively analyze projectspecific data/systems to ensure accuracy and efficiency
• Strong customer focus
• Flexibility to reprioritize workload to meet changing project timelines
• Proven 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 nonclinical/clinical aspects of project implementation and closeout
• Good English language and grammar skills and proficient local language skills as needed
• Advanced digital literacy 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
• Selfmotivated positive attitude and good interpersonal skills

Why Join Us:

We hire the best develop ourselves and each other and recognize the power of being one team. We understand that you will want to grow both professionally and personally throughout your career and therefore you will benefit from an awardwinning learning and development programme ensuring you reach your potential.

What we offer:

As well as being rewarded a competitive salary we have an extensive benefits package based around the health and wellbeing of our employees. We have a flexible working culture where PPD clinical research services truly value a worklife balance. Weve grown sustainably year on year but continue to offer a collaborative environment with teams of colleagues eager to share expertise and have fun together. We are a global organization but with a local feel.

Our Mission is to enable our customers to make the world healthier cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100000 colleagues we share a common set of values Integrity Intensity Innovation and Involvement working together to accelerate research solve complex scientific challenges drive technological innovation and support patients in need. #StartYourStory with PPD part of Thermo Fisher Scientific where diverse experiences backgrounds and perspectives are valued.

Apply today!

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race color religion sex sexual orientation gender identity national origin protected veteran status disability or any other legally protected status.

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