Job Description
job summary:
As the 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. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! location: Telecommute
job type: Contract
salary: $39.00 - 51.65 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- Conduct MLR (Medical, Legal, Regulatory) review of promotional materials to ensure compliance with industry regulations and guidelines.
- Represent medical affairs in the MLR review process.
- Review promotional content for accuracy, efficacy, and safety in accordance with policies and guidelines.
- Support medical initiatives , including MSL activities, medical education, digital communications, and conference preparations.
- Provide medical input on both branded and unbranded content.
- Conduct competitive reviews and publication analyses as needed.
- Collaborate with cross-functional teams to align and execute projects effectively.
- Ensure timely and high-quality completion of assigned projects .
- Attend co-lab meetings (9 AM - 3 PM EST) and contribute to discussions.
- Maintain compliance with internal and external regulatory standards .
qualifications:
Required Skills: - Advanced Scientific Degree (PhD, PharmD, PA, or NP)
- 3+ years of ad/promo medical review experience
- Company Medical Review experience (Veeva promo mat and med-com)
- Strong understanding of MLR processes and compliance
- Scientific understanding of clinical trial data and patient treatment journey
- Excellent oral and written communication skills
- Ability to review promotional materials for accuracy, efficacy, and safety
- Strong analytical and problem-solving skills
- Leadership and collaboration skills with cross-functional teams
- Adaptability to fast-paced environments and changing priorities
Preferred Skills: - Psychiatry/CNS experience
- Previous experience at Abbott or AbbVie (familiarity with expectations and systems)
- Experience in medical affairs and understanding of its functions
- Experience with competitive reviews and publication analyses
- Project management skills for leading medical initiatives
- Ability to support MSL activities, medical education, and digital communications
skills: Drug Safety
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. Randstad
Job Tags
Hourly pay, Contract work, Work experience placement, Remote job,