Global Clinical Training Program Manager (Remote)

Page Mechanical Group, Inc.; San Antonio (TX); Remote; USD 85,000 - 95,000; Full time

Job summary

An innovative organization dedicated to cancer research is seeking a Global Clinical Training Program Manager. This remote position involves coordinating training and development functions across clinical trial sites in the USA and EU. The ideal candidate will have a strong background in clinical research, excellent organizational skills, and a passion for improving patient outcomes. Join a mission-driven team that is transforming cancer treatment through cutting-edge trials and making a real difference in the lives of patients. This is a unique opportunity to contribute to a vital cause while enjoying a flexible work environment and a comprehensive benefits package.

Benefits

Comprehensive health coverage

401(k) plan with employer matching

Life and disability insurance

Health savings and flexible spending accounts

Paid time off

Flexible schedule

Remote work options

Qualifications

• Bachelor's degree in science or equivalent experience required.
• 3+ years in clinical research with training facilitation skills.

Responsibilities

• Develop and implement onboarding plans with Operational Leaders.
• Coordinate monthly START orientation programs and training sessions.
• Conduct audits of training tracking systems for compliance.

Skills

Clinical Research Experience

Training Development

Quality Assurance

Medical Terminology

Office Administration

Education

Bachelor’s degree in science

CCRP or CCRC credentials

Tools

Training Tracking Systems

Computer Applications

Job description

The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START’s mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure. To date, over 43 therapies conducted at START locations have obtained FDA/EMA approval.

Incredibly, while Academic Medical Centers (AMCs) conduct 80% of cancer trials, such trials reach only 20% of the patient population – leaving the majority of patients who are treated in community practices and hospitals without access to a clinical trial when their care journey calls for one. START serves the many – by bringing cancer trials to physicians and their patients in community hospitals and practices when hope is needed most.

START represents the world’s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world.

We are hiring a Global Clinical Training Program Manager. This is a remote role. This role will coordinate the Training & Development functions within the Clinical Quality Assurance Management System (CQMS) for USA and EU network sites. Our preferred candidate will reside in the Central or Eastern time zones.

The annual base salary for this role is $85,000 - $95,000. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience.

Essential Responsibilities:

• Develop and implement pre-boarding and onboarding plans in collaboration with Operational Leaders.
• Plan, coordinate, and facilitate the monthly START orientation program, including scheduling, content maintenance, and tracking completion.
• Facilitate issuance and completion of departmental orientation checklists, self-assessments, and competency reviews under the direction of the CQA Manager.
• Coordinate and facilitate SOP training, including new issuances, revisions, and harmonization initiatives.
• Plan and organize regulatory and maintenance training sessions, including invitations, media dissemination, and internal session coordination.
• Conduct quality checks and audits of training tracking systems to ensure audit readiness and compliance across the network.
• Maintain training needs analysis and prioritization trackers, and report on metrics to the Network Director/Manager of Quality Assurance.

Education & Experience:

• Bachelor’s degree in science or equivalent experience in lieu of degree
• At least three years' experience in clinical research setting
• Ability to accurately establish and facilitate training plans with minimal direction
• General office administration skills, including computer applications, filing systems
• Familiarity with medical terminology, quality assurance and training

Preferred Education and Experience:

• CCRP or CCRC credentials are highly desirable
• Three years of oncology experience preferred

Best-in-Class Benefits and Perks:

We value our employees’ time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

• Comprehensive health coverage: Medical, dental, and vision insurance provided
• Robust retirement planning: 401(k) plan available with employer matching
• Financial security: Life and disability insurance for added protection
• Flexible financial options: Health savings and flexible spending accounts offered
• Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
• Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research:

Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including 43 therapies that were approved by the FDA. START represents the world’s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.

Ready to be part of a team changing the future of cancer treatment?

Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.