Clinical Research Coordinator

Job Description

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.

We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD clinical research services - thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients.

As a Clinical Trial Coordinator, you will play an integral role supporting the Project Team. You will be able to provide administrative and technical support for site activities and coordinate a variety of exciting trials in various therapeutic areas!

Key responsibilities of the Clinical Trial Coordinator are:

• Reviews of regulatory documents for proper content

• Performs PPD investigator file reviews and logging of outstanding issues in project related tracking tools

• Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified

• Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD departments

• Assists with the identification of potential investigators and development/distribution of initial protocol packets

• Creates meeting agendas and minutes

• Coordinates team conference calls and distribution of meeting minutes

To be considered for this exciting opportunity you will require the following skills and experience:

• Some previous administration experience.

• Clinical research knowledge or experience will be seen as an advantage.

• Working skills across all of the Microsoft packages

• Excellent English language and grammar skills

• Strong social skills and high attention for detail, with proven track record to handle multiple tasks efficiently and effectively

Physical Requirements / Work Environment• Frequently stationary for 4-6 hours per day. • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. • Occasional mobility required. • Occasional crouching, stooping, bending and twisting of upper body and neck. • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs. • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.• Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. • May interact with others, relating and gathering sensitive information. Interaction includes diverse groups.• Works with guidance or reliance on oral or written instructions from management. May require periods of intense concentration.