Clinical Project Manager — Remote (GI Trials)

Alimentiv; Houston (TX); Remote; USD 96,000 - 159,000; Full time

Benefits offered by this job

Education Reimbursement

Monthly Cell Phone and Remote Work = “

Office setup allowance

Program: Alimentorship mentorship

Job summary

Alimentiv is seeking a motivated Clinical Project Manager to oversee planning, execution, and delivery of clinical research projects from a home-based setting with occasional travel. You will coordinate cross-functional teams, manage timelines and regulatory compliance, and maintain strong sponsor/client relationships.

The ideal candidate has a Bachelor’s degree in Health Sciences or related field, and 1–3 years of clinical study management experience, with excellent communication and

Qualifications

• Bachelor's degree in Health Sciences, Clinical Research, or related field.
• 1–3 years of clinical study management experience.
• Knowledge of regulatory requirements and study documentation practices.

Responsibilities

• Lead planning, execution, and completion of clinical projects.
• Coordinate cross-functional teams to ensure regulatory compliance.
• Oversee budgets, regulatory requirements, and patient safety.
• Manage study documents and CRFs throughout the life cycle.
• Monitor milestones and provide status updates to sponsors.
• Support site recruitment and stakeholder training initiatives.
• Participate in regulatory submissions and audits.
• Drive communications with sponsors and clients.

Skills

Clinical trial mgmt

Regulatory compliance

Project coordination

Communication skills

Documentation practices

Cross-functional teamwork

Attention to detail

Problem solving

Home-based work readiness

English fluency

Education

Bachelor's degree in Health Sciences

Job description

Alimentiv is seeking a motivated Clinical Project Manager to oversee planning, execution, and delivery of clinical research projects from a home-based setting with occasional travel. You will coordinate cross-functional teams, manage timelines and regulatory compliance, and maintain strong sponsor/client relationships.

The ideal candidate has a Bachelor’s degree in Health Sciences or related field, and 1–3 years of clinical study management experience, with excellent communication and