Senior Clinical Trial Manager Job at Puma Biotechnology Remote Full Time

Remote Clinical Research Opportunity in the Biotechnology Industry

Puma Biotechnology is hiring a Senior Clinical Trial Manager for a full time remote position connected to its operations in Los Angeles. The salary range for this role is between $140000 and $170000 per year depending on experience background and qualifications.

The company is looking for someone with strong experience in clinical trials who can help manage studies from startup through final reporting. Daily work includes handling study timelines coordinating with vendors and research teams reviewing documents and making sure studies follow industry regulations.

People with experience in biotechnology pharmaceutical research or clinical operations may find this position a good fit especially if they already have experience leading clinical studies or managing trial activities across multiple teams.

Job Details Overview

About the Position

The Senior Clinical Trial Manager helps keep clinical studies organized and moving on schedule. The work covers different stages of a study including planning startup tracking timelines vendor coordination and final reporting.

The company wants someone who can stay organized communicate clearly and manage several moving parts at the same time. Some days may include reviewing study documents while other days focus on meetings training sessions or resolving site related issues.

This position also includes regular communication with investigators vendors medical teams and regulatory staff. Since studies can change quickly the person hired for this role should be comfortable handling updates deadlines and unexpected issues when they come up.

Main Responsibilities

The person hired for this position will support daily clinical trial operations and help studies stay on track from beginning to end.

Key duties include:

• Managing clinical trials from startup through completion
• Reviewing study timelines budgets and project milestones
• Coordinating with vendors investigators and research teams
• Reviewing monitoring reports and study documentation
• Supporting site selection and site management activities
• Preparing or reviewing clinical study plans and materials
• Ensuring studies follow GCP and regulatory guidelines
• Assisting with audit preparation and issue resolution
• Leading study meetings and training sessions
• Monitoring protocol deviations and study tracking systems
• Supporting regulatory and ethics committee activities
• Mentoring junior clinical operations staff when needed

The role also includes working closely with medical directors regulatory teams and outside clinical partners throughout different stages of each study.

Education and Experience

The company is searching for someone who can handle busy workloads while staying organized and focused. Clinical trials often involve different departments deadlines and vendors so communication and planning skills are important.

Preferred skills include:

• Strong written and verbal communication
• Ability to manage multiple projects at once
• Leadership and problem solving skills
• Experience working with vendors and research sites
• Understanding of clinical research documents
• Familiarity with spreadsheets and document systems
• Ability to work independently from home

Applicants should also understand clinical trial regulations and industry standards connected to research studies.

Education and Experience Requirements

To qualify for this role applicants usually need a combination of education and professional clinical trial experience.

Required Qualifications

• Bachelor’s degree in science healthcare or a related field
• At least 6 years of clinical trial experience
• Minimum 3 years of clinical trial management experience
• Strong understanding of GCP ICH and regulatory requirements

Preferred Qualifications

• Oncology clinical trial experience
• Experience managing global clinical studies
• Background in pharmaceutical biotech or CRO environments

Candidates with stronger clinical operations backgrounds or advanced experience may qualify for higher compensation depending on skills and location.

Remote Work Environment

This is a fully remote position so most work happens from home. Team communication usually takes place through video meetings email updates and online collaboration tools shared between study teams vendors and research sites.

Even though the position is remote some travel may still be required during certain stages of a study. Travel could include investigator meetings site visits or other clinical trial activities.

Travel responsibilities may include:

• Attending investigator or study meetings
• Visiting research sites when needed
• Carrying laptops or work materials during travel
• Longer travel hours during busy project periods

The regular work schedule follows Monday through Friday. However some evenings or weekends may occasionally be needed depending on study timelines or project deadlines.

Salary and Employee Benefits

The yearly salary for this position ranges from $140000 to $170000. Final pay depends on experience skills qualifications and location.

Along with salary the company may also provide:

• Annual bonus opportunities
• Health and wellness benefits
• Paid time off
• Career development support
• Competitive employee compensation packages
• Remote work flexibility

Benefit packages may vary depending on employment terms and eligibility requirements.

Equal Employment Opportunity

Puma Biotechnology Careers follows equal employment opportunity policies and reviews qualified applicants without discrimination based on race gender religion disability veteran status sexual orientation or other protected categories under law.

The company also mentions that it does not accept unsolicited resumes from outside recruiters or staffing agencies.

How to Apply

Interested applicants can apply through the company’s official careers page or approved job platforms.

Before applying candidates should prepare:

• An updated professional resume
• Details about clinical trial management experience
• Information related to regulatory or oncology experience
• Relevant certifications or qualifications if available

Applications may stand out more when candidates clearly explain their clinical operations background leadership work and experience managing complex studies or research teams.

About Puma Biotechnology

Puma Biotechnology is a biotechnology company focused mainly on cancer research and treatment development. The company works on therapies designed to support patients dealing with serious illnesses especially within oncology care and research.

Clinical operations teams help studies stay organized safe and compliant with research standards. Their work supports the process of developing and testing future medical treatments that may later help patients worldwide.

Final Thoughts

The Senior Clinical Trial Manager opening at Puma Biotechnology may suit experienced clinical research professionals who enjoy managing studies coordinating with different teams and working in a remote setup.

The combination of remote flexibility competitive salary and involvement in oncology research may appeal to candidates with strong clinical operations experience looking for long term work in the biotechnology field.

Disclaimer

This article is shared for informational purposes only. We are not affiliated with the hiring company. Applicants should visit the official Puma Biotechnology careers page for complete job details and application instructions.