Clinical Project Manager

Ladders; United States; Remote; USD 115,000 - 145,000; Full time

Benefits offered by this job

Collaborative work environment

Opportunities for professional develop

Engagement in diverse clinical projcts

Supportive team culture

Access to advanced tools and tech

Job summary

Our client is seeking a Clinical Project Manager to oversee planning and execution of clinical studies, ensuring regulatory compliance, sponsor communications, and cross-functional coordination. You will drive trial milestones, generate status updates, and support audits and inspections with internal teams and external partners.

This remote-US position focuses on study operations, team leadership, and readiness for inspections, with compensation in the provided range.

Qualifications

• Bachelor's degree in life sciences or related field, or equivalent experience.
• 3 years of experience in the pharmaceutical, biotechnology, or CRO industry, including 1 year in a management role.
• Detail-oriented with strong organizational skills.
• Proficient in MS Office Suite, especially Word and Excel.
• Excellent communication and interpersonal skills.

Responsibilities

• Manage clinical research studies to ensure compliance with protocols and regulations.
• Serve as the primary point of contact for study sponsors.
• Oversee clinical study functions including data management and pharmacovigilance.
• Generate and present study status updates to sponsors.
• Supervise and train clinical team members and Associate PMs.
• Facilitate teamwork and communication to meet trial milestones.
• Prepare for and participate in audits and inspections.

Skills

Excellent communication and Interperso

Education

Bachelor's degree in life sciences or related field

Tools

MS Office Suite (Word and Excel)

Job description

For our client, we are seeking a Clinical Project Manager to join the team of a leader in the Pharmaceuticals & Biotech space.

This role will oversee the planning and execution of clinical research studies, with a focus on compliance, sponsor communication, and cross-functional coordination. You will be responsible for keeping trials on track through strong project management, clear status reporting, and effective collaboration with internal teams and external partners. The position also plays an important role in supporting study operations, team leadership, and readiness for audits and inspections.

Location: Remote - US based candidates only, no visa sponsorship available

Compensation: $115,000 – $145,000 annually

Responsibilities

• Manage clinical research studies to ensure compliance with protocols and regulations
• Serve as the primary point of contact for study sponsors
• Oversee clinical study functions including data management and pharmacovigilance
• Generate and present study status updates to sponsors
• Supervise and train clinical team members and Associate PMs
• Facilitate teamwork and communication to meet trial milestones
• Prepare for and participate in audits and inspections

Qualifications

• Bachelor's degree in life sciences or a related field, or equivalent experience
• 3 years of experience in the pharmaceutical, biotechnology, or CRO industry, including 1 year in a management role
• Detail-oriented with strong organizational skills
• Proficient in MS Office Suite, especially Word and Excel
• Excellent communication and interpersonal skills

Benefits

• Collaborative work environment
• Opportunities for professional development
• Engagement in diverse clinical projects
• Supportive team culture
• Access to advanced tools and technologies

Our client is an equal opportunity employer.