Match score not available

Clinical Manager, Clinical Operations - Remote

Remote:

Full Remote

Salary:

139 - 152K yearly

Experience:

Senior (5-10 years)

Work from:

United States

Offer summary

Qualifications:

BS degree in life science, 5 to 10 years clinical experience, 3 years project management experience, Knowledge of US medical device regulations.

Key responsabilities:

Manage clinical studies for evidence generation
Ensure compliance with clinical research regulations
Negotiate clinical site budgets and contracts
Develop and approve monitoring guidelines and training materials

Calyxo, Inc. Startup http://www.calyxoinc.com/

11 - 50 Employees

See all jobs

Job description

Calyxo, Inc. is a medical device company headquartered in Pleasanton, California, USA. The company was founded in 2016 to address the profound need for improved kidney stone treatment. Kidney stone disease is a common, painful condition that consumes vast amounts of healthcare resources each year. Our team is led by executives and investors with a proven track record of commercializing paradigm-shifting devices to meet unmet needs within urology.

Are you ready to change the future of kidney stone treatment? We are seeking high achievers who want to be part of a dynamic team working in a fun, diverse atmosphere.

In This Role, You Will:

Effectively manage clinical studies to support the clinical operation goals that align with the company’s visions for evidence generation
Ensure clinical research is conducted in accordance with 21 CFR Part 812, 50 and 56 and applicable international standards
Independently manage all phases of a clinical study including essential document management, contract review, IRB/EC support, recruitment, site payment reconciliation, and development of site tools
Identify, evaluate and qualify clinical sites to ensure compliance with applicable regulatory regulations
Assist in negotiating clinical site budgets and study contracts
Prepare clinical monitoring guidelines
Generate various study and training materials to support clinical trials
Source, manage and train CRAs assigned to study sites
Review and approve CRA site monitoring trip reports
Conduct site initiation visits and provide clinical trial related training for RCs, Investigators, OR staff, etc.
Provide surgical technique training and proctor clinical cases at hospital and ASC facilities
Plan and conduct investigator meetings
Assist in identifying, evaluating and managing CROs or vendors for study related services including but limited to: data management, statistical analysis, monitoring
Ability to escalate significant issues to senior management in a timely manner, while working to resolve site-specific challenges
Provide technical eDC and clinical support during clinical research
Monitor clinical study data and assist in cleaning of eDC and other study databases
Develop project management tools to manage clinical projects and study tracking tools to report on metrics
Assist with data analysis and summarizing to report to management
Assist with development of clinical strategy, which includes the preparation of clinical protocols and investigational plans.
Other duties may be assigned as a part of job scope

Who You Will Report To:

Director, Clinical Operations

Supervisory Responsibilities:

CRAs (contract and internal)

Requirements:

BS degree in a life science.
5 to 10 years of relevant clinical experience in medical devices.
At least three years of full-cycle clinical project management experience.
Intimate working knowledge of US clinical research and medical device regulations.
Ability to effectively work cross-functionally with multiple departments; manage completion of multiple tasks.
Ability to prioritize projects and display initiative and flexibility.
Detail oriented, strong people and organizational skills.
Strong medical background and understanding of the fundamentals of clinical research and statistical methodology. Background in urology research preferable.
Proficient with PC and associated software. Strong technical, written and communication skills.
Ability to travel up to 50% of the time
Proficiency in Power Point, Excel and eDC platforms

What We Offer:

At Calyxo, you will be part of a knowledgeable, high-achieving, experienced and fun team. You will work in a diverse work environment with experienced, proven leaders and have an opportunity to shape our company culture. You will experience constant learning and dynamic challenges to help you grow and be the best version of yourself.

We also offer a compensation plan as follows:

Competitive base salary of $139,000 - $152,000
Stock options – ownership and a stake in growing a mission-driven company
Employee benefits package that includes 401(k), healthcare insurance and paid time off

Calyxo is deeply committed to fostering an environment where diversity and inclusion are not only valued but also prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways. Diverse viewpoints bring diverse capabilities, which strengthen our focus and fuel our growth.

Calyxo is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status or any other applicable legally protected characteristics

Legal authorization to work in the United States is required. In compliance with federal law, all persons hired will be required to verify their identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.