Clinical Study Manager
Stryker
Portage, MIFull-time
70K–110K a year
Behavioral Health Market Context
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Job Description
y to lead and oversee all aspects of clinical studies, from planning and execution to data analysis and reporting. We are seeking a knowledgeable and collaborative individual with excellent communication skills and a strong background in clinical research. If you are ready to make a meaningful impact in the medical device industry, we want to hear from you!
Lead and oversee all aspects of clinical studies, including protocol development, study design, and execution.
Collaborate with cross-functional teams to ensure study timelines, budgets, and quality standards are met.
Manage and coordinate study activities, including site selection, patient recruitment, and monitoring.
Ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.
Develop and maintain study documents, such as study protocols, informed consent forms, and study reports.
Monitor and analyze study data to identify trends and potential issues.
Communicate study progress, results, and any potential risks to stakeholders, including internal teams and external partners.
Manage relationships with study sites, investigators, and vendors.
Provide guidance and support to study team members and ensure all team members are trained on study procedures and protocols.
Conduct study meetings and trainings as necessary.
Develop and manage study budgets and timelines.
Prepare and submit study-related documents to regulatory authorities.
Stay informed about industry trends and advancements in clinical research.
Ensure all study activities are conducted in accordance with ethical principles and patient safety.
Continuously evaluate and improve study processes to ensure efficiency and quality.
Stryker is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Lead and oversee all aspects of clinical studies, including protocol development, study design, and execution.
Collaborate with cross-functional teams to ensure study timelines, budgets, and quality standards are met.
Manage and coordinate study activities, including site selection, patient recruitment, and monitoring.
Ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.
Develop and maintain study documents, such as study protocols, informed consent forms, and study reports.
Monitor and analyze study data to identify trends and potential issues.
Communicate study progress, results, and any potential risks to stakeholders, including internal teams and external partners.
Manage relationships with study sites, investigators, and vendors.
Provide guidance and support to study team members and ensure all team members are trained on study procedures and protocols.
Conduct study meetings and trainings as necessary.
Develop and manage study budgets and timelines.
Prepare and submit study-related documents to regulatory authorities.
Stay informed about industry trends and advancements in clinical research.
Ensure all study activities are conducted in accordance with ethical principles and patient safety.
Continuously evaluate and improve study processes to ensure efficiency and quality.
Stryker is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Qualifications
- •Do you thrive in a fast-paced environment and have experience managing multiple projects simultaneously?
- •We are seeking a knowledgeable and collaborative individual with excellent communication skills and a strong background in clinical research
Benefits
Responsibilities
- •In this role, you will have the opportunity to lead and oversee all aspects of clinical studies, from planning and execution to data analysis and reporting
- •If you are ready to make a meaningful impact in the medical device industry, we want to hear from you!
- •Lead and oversee all aspects of clinical studies, including protocol development, study design, and execution
- •Collaborate with cross-functional teams to ensure study timelines, budgets, and quality standards are met
- •Manage and coordinate study activities, including site selection, patient recruitment, and monitoring
- •Ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines
- •Develop and maintain study documents, such as study protocols, informed consent forms, and study reports
- •Monitor and analyze study data to identify trends and potential issues
- •Communicate study progress, results, and any potential risks to stakeholders, including internal teams and external partners
- •Manage relationships with study sites, investigators, and vendors
- •Provide guidance and support to study team members and ensure all team members are trained on study procedures and protocols
- •Conduct study meetings and trainings as necessary
- •Develop and manage study budgets and timelines
- •Prepare and submit study-related documents to regulatory authorities
- •Stay informed about industry trends and advancements in clinical research
- •Ensure all study activities are conducted in accordance with ethical principles and patient safety
- •Continuously evaluate and improve study processes to ensure efficiency and quality
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