Aroga Biosciences
Regulatory Medical Writer (Manager to Director Level)
Aroga Biosciences, San Diego, California, United States, 92189
Overview
Aroga Biosciences is an award-winning Contract Research Organization (CRO) based in San Diego, CA. We specialize in providing regulatory writing and submission services for biotech and pharmaceutical projects. Our team has extensive regulatory and medical writing experience across therapeutic areas, and we are committed to delivering high-quality deliverables while maintaining flexibility and adherence to regulatory standards. Role Description This is a full-time hybrid role for a Regulatory Medical Writer (levels up to Director). The Regulatory Medical Writer will develop high-quality regulatory documents (e.g., clinical study reports, clinical protocols, and Investigator’s Brochures). The position requires collaboration with cross-functional teams, reviewing and interpreting data, and ensuring compliance with regulatory guidelines. While primarily based in San Diego, CA, there is flexibility for some remote work. Responsibilities
Develop regulatory documents such as clinical study reports, clinical protocols, and Investigator's Brochures. Collaborate with cross-functional teams and interpret data to ensure regulatory compliance. Review and interpret data, ensuring adherence to regulatory guidelines and requirements. Qualifications
Master’s or doctoral degree (M.S., Ph.D., Pharm.D, M.D., or equivalent) Scientific Writing, Medical Communications, and/or Medical Writing experience Experience writing and reviewing regulatory documents Strong research and analytical skills Excellent written and verbal communication skills Attention to detail and ability to meet tight deadlines Knowledge of regulatory guidelines and requirements Experience in the biotech or pharmaceutical industry is a plus Senior-level candidates should have management/mentorship experience Benefits and Perks
Competitive salary; salary and position commensurate with experience Comprehensive medical, dental, and vision insurance Flexible work week Hybrid schedule – onsite with option to work remotely on Mon and Fri Remote employment may be considered with 10% travel 401(k) options Location
San Diego, CA Seniority level
Mid-Senior level Employment type
Full-time Job function
Regulatory Writing and Medical Writing
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Aroga Biosciences is an award-winning Contract Research Organization (CRO) based in San Diego, CA. We specialize in providing regulatory writing and submission services for biotech and pharmaceutical projects. Our team has extensive regulatory and medical writing experience across therapeutic areas, and we are committed to delivering high-quality deliverables while maintaining flexibility and adherence to regulatory standards. Role Description This is a full-time hybrid role for a Regulatory Medical Writer (levels up to Director). The Regulatory Medical Writer will develop high-quality regulatory documents (e.g., clinical study reports, clinical protocols, and Investigator’s Brochures). The position requires collaboration with cross-functional teams, reviewing and interpreting data, and ensuring compliance with regulatory guidelines. While primarily based in San Diego, CA, there is flexibility for some remote work. Responsibilities
Develop regulatory documents such as clinical study reports, clinical protocols, and Investigator's Brochures. Collaborate with cross-functional teams and interpret data to ensure regulatory compliance. Review and interpret data, ensuring adherence to regulatory guidelines and requirements. Qualifications
Master’s or doctoral degree (M.S., Ph.D., Pharm.D, M.D., or equivalent) Scientific Writing, Medical Communications, and/or Medical Writing experience Experience writing and reviewing regulatory documents Strong research and analytical skills Excellent written and verbal communication skills Attention to detail and ability to meet tight deadlines Knowledge of regulatory guidelines and requirements Experience in the biotech or pharmaceutical industry is a plus Senior-level candidates should have management/mentorship experience Benefits and Perks
Competitive salary; salary and position commensurate with experience Comprehensive medical, dental, and vision insurance Flexible work week Hybrid schedule – onsite with option to work remotely on Mon and Fri Remote employment may be considered with 10% travel 401(k) options Location
San Diego, CA Seniority level
Mid-Senior level Employment type
Full-time Job function
Regulatory Writing and Medical Writing
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