Join a high-impact medical affairs team working on meaningful clinical and scientific initiatives that directly support product strategy, education, and commercialization. This remote opportunity is tied to a major biopharma company's North Chicago campus and offers the chance to lead key efforts in medical review, data dissemination, and scientific alignment across internal and external stakeholders. If you have experience in medical and promotional review processes, particularly using platforms like Veeva PromoMats, this role offers a unique opportunity to influence decision-making and strategic execution in a fast-paced, matrixed environment.
This role is ideal for a detail-oriented professional with deep therapeutic knowledge, a scientific degree (advanced preferred), and a background in regulatory-compliant medical communications. You'll collaborate cross-functionally while independently managing high-value medical content and strategy execution in support of disease state education, clinical data, and commercial alignment.
location: Telecommute
job type: Contract
salary: $40.00 - 46.74 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- Contribute to therapeutic area strategy and medical education tactics
- Lead execution of advisory boards, thought leader engagement, and conference planning
- Represent the company at external meetings, including investigator and association events
- Provide medical review of labels, clinical data, and disease state content
- Train others on medical review processes
- Manage budgets and vendor relationships for assigned projects
- Support generation and dissemination of clinical/scientific data
- Perform competitive assessments and scientific literature reviews
- Align initiatives with the Scientific Communication Platform
- Assist in creating and training on Medical Information (MI) materials
- Participate in launch readiness planning
qualifications:
Required Skills & Qualifications:
- Scientific degree required; advanced degree (MS, PhD, MD/DO, PharmD, NP, MSN) strongly preferred
- 3-5 years of relevant clinical, research, or industry experience
- Experience performing medical review of both medical and promotional materials
- Familiarity with Veeva PromoMats and/or MedComms systems
- Ability to quickly grasp and work within various therapeutic areas, including AML
- Clear and concise communication of review rationale to cross-functional teams
- Strong leadership, teamwork, and matrix collaboration skills
- Experience with medical affairs strategy and external communication alignment
- Understanding of legal/regulatory guidelines (FDA, OPDP, HIPAA, GCP, ICH, etc.)
- Knowledge of clinical trial design, study publications, and regulatory documentation
- Comfort leading projects and influencing without direct authority in a global team setting
skills: Drug Safety, ICH Regulations, International Council for Harmonization (ICH), HIPAA Compliance
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: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (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.
