Clinical Trial Manager

Ladders; United States; Remote; USD 110.000 - 130.000; Vollzeit

Benefits dieser Stelle

Health coverage

Retirement plan

Life insurance

Wellbeing resources

Training programs

Zusammenfassung

Ladders is seeking a Clinical Trial Manager to oversee end-to-end clinical study planning and execution. The role emphasizes timelines, budgets, and deliverables, working with investigators, vendors, and cross-functional teams to maintain protocol alignment and regulatory compliance.

The position is remote for US-based candidates, with travel up to ~25%. Compensation ranges from $110,000 to $130,000 annually, reflecting experience and responsibilities in a fast-paced pharmaceutical environment.

Qualifikationen

• University degree in medicine, science, or equivalent education/experience.
• Proven ability to drive clinical study deliverables.
• Expertise in the designated therapeutic area.
• Prior monitoring experience preferred.
• Willingness to travel approximately 25% of the time.

Aufgaben

• Plan and manage all aspects of clinical trials, ensuring timelines and budgets are met.
• Collaborate with cross-functional teams to implement trial protocols.
• Build and maintain relationships with trial investigators and stakeholders.
• Ensure compliance with local, national, and international regulations.
• Problem-solve and make decisions regarding trial design and vendor selection.

Kenntnisse

Clinical trial mgmt

Regulatory awareness

Vendor management

Travel readiness

Ausbildung

University degree in medicine/science/experiences

Jobbeschreibung

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

This role will oversee the planning and execution of clinical studies from start to finish, with a strong focus on timelines, budgets, and study deliverables. You will partner closely with cross-functional internal teams, investigators, vendors, and other stakeholders to keep trials moving forward and aligned with protocol requirements. Success in this role will depend on strong regulatory awareness, sound decision-making, and the ability to manage complex study activities in a fast-paced clinical research environment.

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

Compensation: $110,000 – $130,000 annually

Responsibilities

• Plan and manage all aspects of clinical trials, ensuring timelines and budgets are met
• Collaborate with cross-functional teams to implement trial protocols
• Build and maintain relationships with trial investigators and stakeholders
• Ensure compliance with local, national, and international regulations
• Problem-solve and make decisions regarding trial design and vendor selection

Qualifications

• University degree in medicine, science, or equivalent education/experience
• Proven ability to drive clinical study deliverables
• Expertise in the designated therapeutic area
• Prior monitoring experience preferred
• Willingness to travel approximately 25% of the time

Benefits

• Comprehensive health and wellbeing programmes including medical, dental, and vision coverage
• Retirement and pension plans included
• Life assurance and disability coverage provided
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training

Our client is an equal opportunity employer.