Medical Writer at Rose International

The Medical Affairs Writer supports the department in coordinating medical training and compliance-related tasks, provide group support in medical writing and administration of research, partnerships, and HCPs (healthcare providers) contracts.

EDUCATION REQUIREMENTS
•B.S in a biomedical science discipline (e.g. pharmacology, biology, biochemistry, pharmacy, medical sciences), preferably with one or more years of work experience in a biomedical setting

REQUIRED SKILLS
•Ability to see and comprehend the big picture of a project team, yet thorough and attentive to the intricate details of the scientific work
•Being resourceful and possessing good problem-solving skills to resolve issues, reach project objectives and milestones on time
•Ability to work in a multistakeholder, multidisciplinary setting with Medical Directors, Compliance, Procurement, and other business functions
•Self-motivated person focused on delivering team/project outcomes
•Excellent verbal and written communication skills, with the willingness to learn new tools and approaches
•Demonstrated proficiency in using and agility in learning business applications such as Word, Excel, PowerPoint, MS TEAMS, MS AI copilot

POSITION SUMMARY
Reporting to the VP of US Medical Affairs, the Medical Writer will be supporting needs arise within the US Medical Affairs team, including the medical directors.

RESPONSIBILITIES
•Perform medical writing to support scientific publications, medical training programs, and conduct internal publication clearance for the US medical affairs department
•Support the VP of US Med Aff on local medical governance-related activities such as compliance tracking, local standard operating procedure updates and roll out to meet compliance requirements
•Support the coordination of medical inquires, medical or product research, and fellowship programs
•Help set agenda and scheduling with goals to build capabilities and performance excellence and efficiency of the team
•Oversee and administer all department contracts and purchase orders including those with scientific thought leaders, healthcare providers, vendors, clinical study sites, and advisory boards
•Facilitate fair market value assessment and ensure contractual compliance by interfacing with procurement and legal departments
•Other administrative tasks to support the collective team

***Drug screen & criminal background check will be required

Benefits:

For information and details on employment benefits offered with this position, please visit here .Should you have any questions / concerns, please contact our HR Department via our secure website .

California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.

Rose International is an Equal Opportunity Employer.All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender(expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law.Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.

If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.

Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).