Senior Clinical Trial Manager
Senior Clinical Trial Manager Needed
Description:
Responsible for leading global clinical trials from start up through closure (internally sourced studies and studies outsourced to CROs).
Direct Management and oversight of third-party vendors and CROs.
Experience driving process improvement initiatives. Will be responsible for developing study specific documentation (Case report forms - CRFs, data management plans, monitoring plans, monitoring oversight plans, data review plan, statistical analysis plan, etc.
Responsible for leading risk assessments and identifying risk mitigation strategies at the study level.
Directly supervising Clinical Trial Management staff, including assigning work, performance management, recruitment, mentoring and professional development
Management of vendors and CROs
CTMS & TMF System - Veeva Vault - supervising setup and maintenance of study teams
Providing input into baseline budget and timeline development and managing the study against planned budget, timeline and results
Additional Skills &
Qualifications:
Bachelors Degree
8
years of experience LEADING GLOBAL Clinical trials within Pharma Industry
6
years of experience managing and overseeing CRO's and vendors
looking for someone who shows a lot of drive and energy and can handle large workload, attention to detail very important
Experience Level:
Expert Level
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.Estimated Salary: $20 to $28 per hour based on qualifications.
Description:
Responsible for leading global clinical trials from start up through closure (internally sourced studies and studies outsourced to CROs).
Direct Management and oversight of third-party vendors and CROs.
Experience driving process improvement initiatives. Will be responsible for developing study specific documentation (Case report forms - CRFs, data management plans, monitoring plans, monitoring oversight plans, data review plan, statistical analysis plan, etc.
Responsible for leading risk assessments and identifying risk mitigation strategies at the study level.
Directly supervising Clinical Trial Management staff, including assigning work, performance management, recruitment, mentoring and professional development
Management of vendors and CROs
CTMS & TMF System - Veeva Vault - supervising setup and maintenance of study teams
Providing input into baseline budget and timeline development and managing the study against planned budget, timeline and results
Additional Skills &
Qualifications:
Bachelors Degree
8
years of experience LEADING GLOBAL Clinical trials within Pharma Industry
6
years of experience managing and overseeing CRO's and vendors
looking for someone who shows a lot of drive and energy and can handle large workload, attention to detail very important
Experience Level:
Expert Level
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.Estimated Salary: $20 to $28 per hour based on qualifications.
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