Hello prospective Clinical Study Manager candidates,Are you a driven and detail-oriented individual with a passion for improving patient outcomes through clinical research? Do you thrive in a fast-paced environment and have experience managing multiple projects simultaneously? If so, Stryker is looking for you to join our team as a Clinical Study Manager. 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. 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.
A Bachelor's Or Master's Degree In A Relevant Field Such As Clinical Research, Healthcare Administration, Or Life Sciences.
At Least 5 Years Of Experience In Clinical Research, Preferably In A Managerial Role.
In-Depth Knowledge Of Fda Regulations And Ich/Gcp Guidelines.
Excellent Project Management Skills, Including The Ability To Plan, Organize, And Oversee Multiple Clinical Trials Simultaneously.
Strong Communication And Interpersonal Skills, With The Ability To Effectively Collaborate With Cross-Functional Teams And Build Relationships With External Stakeholders.
Communication Skills
Project Management
Vendor Management
Data Analysis
Time Management
Budget management
Team Leadership
Risk assessment
Regulatory compliance
Resource allocation
Protocol Development
Clinical Operations
Communication
Conflict Resolution
Customer Service
Emotional Intelligence
Leadership
Problem Solving
Time management
creativity
Teamwork
Adaptability
According to JobzMall, the average salary range for a Clinical Study Manager in Portage, MI, USA is $70,000-$110,000 per year. This can vary depending on factors such as experience, education, and specific job responsibilities. Some Clinical Study Managers may earn more or less than this range.
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Stryker Corp. is engaged in providing medical technology products and services. It operates through the following segments: Orthopaedics, MedSurg and Neurotechnology and Spine. The Orthopaedics segment provides reconstructive and trauma implant systems. The Medsurg segment deals with surgical instruments and equipment, endoscopy, patient handling, and reprocessed medical devices. The Neurotechnology and Spine segment pertains to spinal implants and neurovascular products.
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