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Senior Clinical Trial Manager
2 months ago
About Us
Worldwide Clinical Trials, LLC is a leading global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality.
Our company's scientific heritage is anchored in our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, which enables us to develop flexible plans and solve problems quickly for our customers.
We have a talented team of 3,000+ professionals spanning 60+ countries, united in our cause to improve the lives of patients through new and innovative therapies.
Our Culture
We believe that everyone plays an important role in making a world of difference for patients and their caregivers. Our hands-on, accessible leaders and cohesive, supportive teams are committed to enabling professionals from all backgrounds and experiences to succeed.
We prioritize cultivating a diverse and inclusive environment that promotes collaboration and creativity, where people thrive by being themselves and are inspired to do their best work every day.
Our Work
As a Clinical Operations Site Management professional at Worldwide Clinical Trials, LLC, you will embark on a fulfilling career that leaves a lasting impact on patients' lives. You will drive extraordinary scientific breakthroughs and contribute to the very heart of every successful clinical trial.
Working alongside brilliant minds across a variety of therapeutic areas, you will have the chance to collaborate closely with top-tier colleagues from diverse backgrounds and specialties.
Our commitment to advancing clinical research is cultivated in a supportive, team-oriented atmosphere, with our hands-on leadership and dedicated team members working together to innovate and solve complex challenges for our customers.
Your Responsibilities
- Provide leadership and direction to clinical site management team members from study start through to closure.
- Serve as Site Management primary point of contact and representative for clinical monitoring and site activities within the project, including:
- Primary Sponsor contact
- Investigator and Bid Defense Meetings
- Internal and External study team calls
- Project-specific Audits / Inspections
- Manage monitoring deliverables to achieve study budget and identify Out of Scope Activities.
- Oversee compliance to the Clinical Monitoring Plan, including site visits, outstanding trip reports, and visit follow-up letters.
Your Qualifications
- Excellent interpersonal, oral, and written communication skills in English and in local language.
- Ability to lead and motivate a team remotely.
- Demonstrate initiative and problem-solving skills by offering solutions when obstacles are identified.
- Strong customer focus, ability to interact professionally within a sponsor contact.
- Proficiency in Microsoft Office, CTMS, and EDC Systems.
Your Experience
- Bachelor's Degree or a Nursing Degree required.
- 1+ years' experience as a Clinical Trial Manager, Clinical Operations Leader, Lead CRA, or equivalent role.
- 3+ years' experience as a Clinical Research Associate.
- Willingness to travel.
