Emerging Clinical Study Manager (Global Trials)

Worldwide Clinical Trials; Texas; On-site; USD 27,000 - 55,000; Full time

Job summary

Worldwide Clinical Trials seeks an Associate Clinical Study Manager to oversee site-level monitoring across Phase I–IV trials, coordinating with the CSM and functional leads to ensure on-time, quality deliverables.

The role requires strong communication, planning, and problem-solving abilities, with the ability to work independently and liaise with clients professionally. A Life Sciences degree or equivalent clinical research experience is preferred.

Qualifications

• Bachelor’s Degree (Life Sciences or Health preferred) or 4 years clinical research experience.

Responsibilities

• Coordinate study monitoring visits and ensure access to relevant systems.
• Collaborate with clinic departments to answer queries promptly.
• Manage signed forms for Clinical Lab, PK processing, and training access.
• Coordinate signature forms for SIV attendance and protocol training meetings.
• Ensure staff training is documented per study protocol and GCP standards.
• Facilitate shipment of samples to bioanalytical labs per timeline.

Skills

Communication

Planning

Organization

Problem-solving

Independent work

Client liaison

Customer service

Education

Bachelor’s Degree or 4 years clinical research experience

Job description

Worldwide Clinical Trials seeks an Associate Clinical Study Manager to oversee site-level monitoring across Phase I–IV trials, coordinating with the CSM and functional leads to ensure on-time, quality deliverables.

The role requires strong communication, planning, and problem-solving abilities, with the ability to work independently and liaise with clients professionally. A Life Sciences degree or equivalent clinical research experience is preferred.