What are the responsibilities and job description for the Senior manager, global medical affairs resource position at Randstad?
job summary :
As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!
location : Telecommute
job type : Contract
salary : $48.17 - 56.67 per hour
work hours : 9 to 5
education : Masters
responsibilities : Duties :
The primary responsibility of this role is to develop and maintain a patient-specific clinical trials website. The ideal candidate will have the ability to work independently and possess experience in medical writing for both patient-specific audiences and scientific audiences.
- Write and edit content for both patient-specific audiences and scientific audiences, ensuring accuracy and clarity.
- Develop and maintain a patient-specific clinical trials website. Ensure the website is user-friendly, informative, and accessible to patients seeking clinical trial information.
- Monitor website analytics and user feedback to continuously improve content and user experience.
- Collaborate cross-functionally to develop scientific content and resources, including scientific / clinical slide decks, educational and training materials, field resources for external use and digital omnichannel assets.
- Develop project timelines and ensure on-time delivery of resources; effectively communicate project timelines and project status to stakeholders
- Manage vendors as needed
- Manage all technical aspects of Medical Review Committee (MRC) reviews and approvals, including annotations, referencing, and comment adjudication, in collaboration with clinical subject matter experts and MRC members and administrators
- Adhere to SOPs, work instructions, and quality standards
- Apply legal, regulatory, and compliance requirements to all Medical Affairs activities
qualifications : Skills
Required
Additional
Education
skills : Project Management
Equal Opportunity Employer : Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).
This posting is open for thirty (30) days.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Salary : $48 - $57
