Remote GI Clinical Project Manager

Alimentiv; Dallas (TX); A distancia; USD 96.000 - 159.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Education reimbursement

Cell phone and remote work allowance

Office setup allowance

Visiting program (up to 4 weeks)

Flexible summer hours

Employee referral incentive

Alimentiv Trust eligibility

Mentorship program

Descripción de la vacante

Alimentiv, a global CRO, 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 budgets, ensure regulatory compliance, and maintain sponsor relationships.

The ideal candidate has 1–3 years of clinical study management experience, strong communication skills, and a detail-oriented, problem-solving mindset to ensure

Formación

• Bachelor's degree in a relevant field, preferably Health Sciences, Clinical Research, or a related discipline.
• 1–3 years of experience in clinical study management, with exposure to clinical research project coordination and execution.
• Strong understanding of clinical research processes, regulatory requirements, quality standards, and study documentation practices.
• Excellent project management and organizational skills, with the ability to coordinate multiple tasks, track deliverables, and meet project deadlines.
• Strong written and verbal communication skills, with the ability to interact effectively with sponsors, clients, investigators, and cross-functional teams.
• Demonstrated ability to build collaborative working relationships, encourage teamwork, and coordinate interdisciplinary project activities.
• Exceptional attention to detail, with a commitment to maintaining accuracy, compliance, and high-quality project outcomes.
• Self-motivated and results-oriented, with strong problem-solving skills and the ability to proactively identify and address project challenges.
• Commitment to continuous learning, professional development, and adapting to evolving project and organizational requirements.
• Fluency in English, including reading, writing, and speaking, with the ability to work effectively in a home-based environment and travel occasionally as required.

Responsabilidades

• Lead the planning, execution, monitoring, and completion of assigned clinical research projects, ensuring project objectives and deliverables are achieved.
• Coordinate cross-functional project teams to ensure activities comply with applicable regulations, industry guidelines, corporate policies, and quality standards.
• Oversee project operations, budgets, regulatory requirements, and patient safety to maintain operational and financial integrity throughout the project life cycle.
• Manage the development, maintenance, and appropriate disposal of essential clinical study documents, data, equipment, and tools, including protocols, SOPs, informed consent forms, and case report forms (CRFs).
• Assign, track, and oversee interdisciplinary activities, including site monitoring, database development, data collection, adverse event management, statistical analysis, and clinical study reporting.
• Serve as the primary point of contact for sponsors and clients, proactively managing expectations, resolving project-related issues, and maintaining effective communication.
• Organize and facilitate project meetings, prepare investigator updates, and provide regular project progress and status reports to relevant stakeholders.
• Support site and patient recruitment strategies, stakeholder training initiatives, and the development of study-related communication materials.
• Participate in regulatory submissions, audits, third-party vendor selection, and other activities required to support successful project delivery.
• Monitor team performance, project milestones, and deliverable quality to ensure alignment with sponsor expectations, project requirements, and regulatory standards.

Conocimientos

Clinical project management

Regulatory compliance

Cross-functional coordination

Communication skills

Documentation practices

Problem-solving

Educación

Bachelor's degree in Health Sciences/Clinical Research

Descripción del empleo

Alimentiv, a global CRO, 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 budgets, ensure regulatory compliance, and maintain sponsor relationships.

The ideal candidate has 1–3 years of clinical study management experience, strong communication skills, and a detail-oriented, problem-solving mindset to ensure