Job Details

ID #50780559
Estado Ohio
Ciudad Akron
Full-time
Salario USD TBD TBD
Fuente ThermoFisher Scientific
Showed 2023-12-31
Fecha 2024-01-01
Fecha tope 2024-03-01
Categoría Etcétera
Crear un currículum vítae

Clinical Research Coordinator

Ohio, Akron, 44301 Akron USA

Vacancy caducado!

Job DescriptionAt 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 – To enable 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. Alongside clinical research through our PPD® clinical research portfolio, our work in accelerated enrollment solutions optimizes each step of the patient journey in clinical trials, such as securing sites and recruiting patients, allowing for more patients to participate in clinical research. Your determination to put patients at the heart of every decision will improve health outcomes that people and communities depend on – now and in the future.NOTE: This position is full-time office-based in Akron, OH (no relocation assistance is provided for this position).#AES#SponCRGDiscover Impactful Work:As a Clinical Research Coordinator you will be a key member impacting the development and research for therapeutics for patients.A day in the Life:

Conducts clinical studies according to FDA/GCP and ICH regulations and guidelines.

Provides medical care to patients, always ensuring patient safety comes first. Performs all defined study activities (i.e, informed consent, screening, and protocol procedures which include but not limited to vital signs, pregnancy tests, height, weight, ECG's, etc.).

Records all patient information and results from tests as per protocol on required forms.

Where required, may complete IP accountability logs and associated information.

Reports suspected non-compliance to relevant site staff.

Ensures that IRB approval is obtained prior to study initiation and IRB requirements are met throughout the study.

Promotes the company and builds a positive relationship with patients to ensure retention.

Attends site initiation meetings and all other relevant meetings to receive training on protocol.

May be required to call patients, do patient bookings and follow-up calls to confirm bookings or provide information or results.

Logs/completes information on sponsor systems and ensures all information provided is accurate (i.e., case report forms, EDC, etc.) and ensures it is completed within timeframe.

Gathers source documents, updates patient files and notes, always ensuring relevant and most up to date information is recorded.

Adheres to company COP/SCOP.

Keys to Success:Education

Bachelor's degree or equivalent and relevant formal academic / vocational qualification in the clinical /medical field

Experience

Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years’)

Knowledge, Skills, Abilities

Basic understanding of the clinical research process (i.e., GCP, SOPs, informed consent, safety monitoring, etc.)

Capable of working independently, analyzing and working with attention to detail, processing and prioritizing sensitive complex information and problem solving

Demonstrated ability to exercise discretion and sound judgement

Adequate decision-making, negotiation and influencing skills

Proficient communication skills and English fluency will be an advantage

Proficient organizational skills

Essential proficiency in basic computer applications

Proficient interpersonal skills to work in a team environment

Physical Requirements / Work Environment

Work is performed in an office/ laboratory and/or a clinical environment.

Exposure to biological fluids with potential exposure to infectious organisms.

Exposure to electrical office equipment.

Personal protective equipment required such as protective eyewear, garments and gloves.

Occasional travel, may be domestic or international.

Ability to work in an upright and /or stationary position for 6-8 hours per day.

Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.

Frequent mobility required.

Occasional crouching, stooping, with frequent 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.

Frequently interacts with others to obtain or relate information to diverse groups.

Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence.

Ability to perform under stress.

Ability to multi-task.

Regular and consistent attendance.

BenefitsWe offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!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 100,000+ 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 Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.Apply today! http://jobs.thermofisher.comThermo 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.Accessibility/DisabilityAccessJob Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255. Please include your contact information and specific details about your required accommodation to support you during the job application process.This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.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.

Vacancy caducado!

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