[Hiring] Clinical Trial Manager @Worldwide Clinical Trials

Role Description

Embark on a fulfilling Clinical Operations career as you leave a lasting impact on patients’ lives. Join Worldwide Clinical Trials for an unparalleled CRO experience, where you can 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.

• 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, but not limited to:
  • 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.

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.

Requirements

• Four-year college curriculum or equivalent with a major concentration in biological, physical or health studies and a minimum experience of 3 years as a Senior Clinical Research Associate (or equivalent), OR
• Two-year college curriculum or equivalent education/training (nursing degree or equivalent life science degree preferred) and a minimum experience of 5 years as a Senior Clinical Research Associate, OR
• Minimum 6-month experience functioning as CTM/LCRA (or equivalent); supporting main CTM and coordinating clinical operations activities.
• Willingness to travel.

Benefits

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