Medical Writer: Clinical Trials and Regulatory Docs

R&D Partners; Los Angeles (CA); On-site; USD 60,000 - 65,582; Full time

Benefits offered by this job

Medical insurance PPO, HMO & HSA

Dental & Vision insurance

401k plan

Employee Assistance Program

Long-term disability

Weekly payroll

Expense reimbursement

Online timecard approval

Job summary

R&D Partners is looking for a Medical Writer in Los Angeles, CA. This role involves supporting the development of clinical trial materials, conducting literature reviews, and collaborating with cross-functional teams to ensure compliance with medical research standards.

The ideal candidate will have 2-4 years of relevant experience and a Bachelor's degree in life sciences or healthcare. Benefits include medical, dental, vision insurance, a 401k plan, and more.

Qualifications

• 2-4 years of experience in clinical research, medical affairs, or regulatory affairs.
• Experience preparing materials for Promotional Review Committees.
• Strong understanding of clinical trial processes and regulatory requirements.

Responsibilities

• Support the development of clinical trial education materials.
• Conduct comprehensive literature reviews.
• Work with cross-functional teams for compliance and accuracy.

Skills

Clinical research

Medical communications

Regulatory affairs

Literature reviews

Education

Bachelor's degree in life sciences

Advanced degree preferred

Job description

R&D Partners is looking for a Medical Writer in Los Angeles, CA. This role involves supporting the development of clinical trial materials, conducting literature reviews, and collaborating with cross-functional teams to ensure compliance with medical research standards.

The ideal candidate will have 2-4 years of relevant experience and a Bachelor's degree in life sciences or healthcare. Benefits include medical, dental, vision insurance, a 401k plan, and more.