Senior Clinical Research Associate - CNS - MidAtlantic/Northeast - Remote Job at Worldwide Clinical Trials - USA, Remote

N2w0dS8vZFBzSzRYeXNmb2JJb1NCWjF0L0E9PQ==
  • Worldwide Clinical Trials - USA
  • Remote

Job Description

Who we are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!

What the Clinical Operations Department does at Worldwide

Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve.

These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role on every clinical trial. All CROs will promise you growth, opportunity and maybe even a challenge. But we offer more than that. We offer an uncommon experience - one you can’t get anywhere else, with a team unlike anyone else.

At Worldwide we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every trial like a patient’s life depends on it - because it does. Our leaders are in the trenches with you daily - committed to advancing science and moving mountains for our customers.

What you will do

  • Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects, which are predominantly registries and other types of non-interventional / observational studies

  • Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded

  • Conduct study initiation visits (SIVs)

  • While most of the site management efforts will be performed remotely, will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirement

What you will bring to the role

  • Excellent interpersonal, oral, and written communication skills in English

  • Superior organizational skills with attention to details

  • Ability to work with little or no supervision

  • Proficiency in Microsoft Office, CTMS and EDC Systems

Your experience

  • 5+ years of experience as a Clinical Research Associate

  • 4-year university degree or RN/BSN in Nursing

  • Willingness to travel required

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide !For more information on Worldwide, visit or connect with us on LinkedIn .

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative,innovative,and successful. We’reon a mission to hire thevery bestand are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law .

Job Tags

Remote job, Permanent employment, Worldwide,

Similar Jobs

BarkandBoarding

Dog Groomer Job at BarkandBoarding

 ...Position: Grooming Reports to: General Manager, Grooming Manager Purpose This position requires an enthusiastic, patient approach to dealing with the pets; ability to learn and adhere to the Bark + Boardings standards and procedures; humane treatment of the animals... 

Capital One

Part Time Branch Ambassador - West Bank Area Job at Capital One

Part Time Branch Ambassador - West Bank Area The Reimagined Branch Experience: Welcome to a new idea in banking. Here at Capital One, were redefining how people bank. You see, we believe banking should fit our customers everyday livesnot the other way around... 

Arthur Lawrence

SAP SD Techno-Functional Consultant Job at Arthur Lawrence

 ...Job Title: SAP SD Techno-Functional Consultant Location: Houston, TX Type of Position: 6-month Contractual Environment: Onsite About the Job: We are seeking an experienced SAP SD Consultant with a strong blend of technical expertise and functional understanding... 

IQVIA

(Senior) Clinical Research Associate - Sponsor Dedicated Job at IQVIA

 ...and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference...  ...4 years of year of on-site monitoring experience.- Equivalent combination of education,...  ...skill in applying, applicable clinical research regulatory requirements, i.e., Good Clinical... 

A & R Transport

CDL-A Truck Drivers Home Daily / Often Job at A & R Transport

CDL-A Truck Drivers Home Daily / OftenHome Most Weekends Avg $1400+ per wkFull Benefits Assigned Late Model TrucksAlso Needing Owner Operators For TopPaying Liquid Loads Plate Program 100% FSC$15k Sign-on for Owner OperatorsTank & Hazmat EndorsementImmediate...