Job Description - Associate Site Manager (2406226391W)
Associate Site Manager - 2406226391W
Description
Associate Site Manager Location: United Kingdom We are looking for a driven Associate Site Manager to serve as the primary contact point between J&J Research & Development and the Investigational Site for trials in phases 2-4. In other organisations, the Associate Site Manager may be known as Clinical Research Associate or Monitor. The head office location is in High Wycombe, Buckinghamshire, and this position is home-based. We are hiring for several therapeutic areas; preferably the candidate will have experience in either Haematology Oncology, Solid Oncology, Immunology or Ophthalmology.
As an Associate Site Manager, you have to ensure inspection readiness and compliance with the clinical trial protocol, Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations from study start-up through to site closure. We need a flexible Associate Site Manager who is able to work independently as well as part of a team, a quick learner, a problem solver, and a good communicator. You will collaborate with a Local Trial Manager (LTM), a Clinical Trial Assistant (CTA), and a Clinical Trial Manager (CTM) to perform trial-related activities for assigned protocols and sites. You are responsible for the overall site management activities. You will be part of a hardworking, enthusiastic, and committed team eager to deliver and help improve the lives of millions of patients.
Responsible for activities ranging from site feasibility and selection, site initiation and start-up, to preparation and conduct of site monitoring, oversight of key performance indicators and site/study close-out.
Responsible for the implementation of a site-level analytical risk-based monitoring model and for working with the site to ensure timely resolution of issues and deviations identified during monitoring visits.
Ensure accuracy and completeness of all trial data including safety data. Manage timely data entry and query resolution in collaboration with site staff.
Contribute to site-level recruitment and retention strategies and implementation of mitigation actions in partnership with other functional areas.
Ensure full documentation of trial related activities in all study files; communicates site and study progress and issues to the Local Trial Manager and central study teams.
Be the local expert on your assigned protocols and build the necessary therapeutic area expertise.
Opportunity to be a participant in process improvement and training.
Education and Experience Requirements :
A minimum of a BA or BS degree in Life Sciences, Nursing or related scientific field (or equivalent experience) is required
A minimum of 2 years of clinical trial monitoring experience is preferred, however, other relevant working experiences and skills may be considered by the hiring manager
Knowledge of several therapeutic areas is an asset
Strong proven understanding of GCP, local laws, and regulations
Strong IT skills and ability to operate and use various systems and databases
Ability to establish a home office
Strong team member and self-starter with the ability to work independently
Strong communication and influencing skills to effectively manage study sites both remotely and face-to-face.
Willingness to travel up to 50% (up to 2-3 days per week) with some overnight stays as necessary
We offer a competitive salary and extensive benefits package. The health and well-being of our employees is a priority, we have a flexible working environment as we value work-life balance. We offer career development opportunities for those who want to grow and be part of our organization.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
Primary Location Europe/Middle East/Africa-United Kingdom-England-High Wycombe
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Associate Site Manager - 2406226391W
Description
Associate Site Manager Location: United Kingdom We are looking for a driven Associate Site Manager to serve as the primary contact point between J&J Research & Development and the Investigational Site for trials in phases 2-4. In other organisations, the Associate Site Manager may be known as Clinical Research Associate or Monitor. The head office location is in High Wycombe, Buckinghamshire, and this position is home-based. We are hiring for several therapeutic areas; preferably the candidate will have experience in either Haematology Oncology, Solid Oncology, Immunology or Ophthalmology.
As an Associate Site Manager, you have to ensure inspection readiness and compliance with the clinical trial protocol, Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations from study start-up through to site closure. We need a flexible Associate Site Manager who is able to work independently as well as part of a team, a quick learner, a problem solver, and a good communicator. You will collaborate with a Local Trial Manager (LTM), a Clinical Trial Assistant (CTA), and a Clinical Trial Manager (CTM) to perform trial-related activities for assigned protocols and sites. You are responsible for the overall site management activities. You will be part of a hardworking, enthusiastic, and committed team eager to deliver and help improve the lives of millions of patients.
Responsible for activities ranging from site feasibility and selection, site initiation and start-up, to preparation and conduct of site monitoring, oversight of key performance indicators and site/study close-out.
Responsible for the implementation of a site-level analytical risk-based monitoring model and for working with the site to ensure timely resolution of issues and deviations identified during monitoring visits.
Ensure accuracy and completeness of all trial data including safety data. Manage timely data entry and query resolution in collaboration with site staff.
Contribute to site-level recruitment and retention strategies and implementation of mitigation actions in partnership with other functional areas.
Ensure full documentation of trial related activities in all study files; communicates site and study progress and issues to the Local Trial Manager and central study teams.
Be the local expert on your assigned protocols and build the necessary therapeutic area expertise.
Opportunity to be a participant in process improvement and training.
Education and Experience Requirements :
A minimum of a BA or BS degree in Life Sciences, Nursing or related scientific field (or equivalent experience) is required
A minimum of 2 years of clinical trial monitoring experience is preferred, however, other relevant working experiences and skills may be considered by the hiring manager
Knowledge of several therapeutic areas is an asset
Strong proven understanding of GCP, local laws, and regulations
Strong IT skills and ability to operate and use various systems and databases
Ability to establish a home office
Strong team member and self-starter with the ability to work independently
Strong communication and influencing skills to effectively manage study sites both remotely and face-to-face.
Willingness to travel up to 50% (up to 2-3 days per week) with some overnight stays as necessary
We offer a competitive salary and extensive benefits package. The health and well-being of our employees is a priority, we have a flexible working environment as we value work-life balance. We offer career development opportunities for those who want to grow and be part of our organization.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
Primary Location Europe/Middle East/Africa-United Kingdom-England-High Wycombe
#J-18808-Ljbffr
