
11 - 50 employees
Founded 2020
📚 Education
🤝 Non-profit
🌍 Social Impact
Education • Non-profit • Social Impact
ResearchEd is an education policy research nonprofit providing objective analysis, deep insights, and detailed recommendations for education institutions and research organizations seeking to support equitable student outcomes and promote community and economic development through education. ResearchEd conducts student-centered work, particularly focusing on underserved groups, and provides research, data capacity building support, and advocacy. Their mission is to empower action in education, aiming for equitable access to education as a catalyst for community success and social justice.
🕒 April 9
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11 - 50 employees
Founded 2020
📚 Education
🤝 Non-profit
🌍 Social Impact
Education • Non-profit • Social Impact
ResearchEd is an education policy research nonprofit providing objective analysis, deep insights, and detailed recommendations for education institutions and research organizations seeking to support equitable student outcomes and promote community and economic development through education. ResearchEd conducts student-centered work, particularly focusing on underserved groups, and provides research, data capacity building support, and advocacy. Their mission is to empower action in education, aiming for equitable access to education as a catalyst for community success and social justice.
• Author and review regulatory & other medical writing deliverables independently • Support in building technical & functional expertise within the group • Contribute/support other writers for manuscripts, slide sets, abstracts, posters, and other techno-commercial documents • Authoring & reviewer of CSRs, Protocol, IB, Briefing books & other regulatory submission documents for US FDA, EMEA and rest of the world • Work with data analysts and statisticians on Real world and evidence generation projects • Undertake quality control (QC, scientific reviews and/or proofreading of deliverables) • Conduct client/KOL interactions, kickoff meetings, and teleconferences • Act as project lead/delivery lead for assigned client • Support innovation initiatives including automation and process improvement • Conduct robust training programs for the team
• Education: PharmD, M. Pharm, PhD, MD, Post-graduate degree in Life science/medical/para medical • At least 10-11 years of experience in medical writing, drug development, clinical research • At least 5 years in core medical writing (regulatory deliverables) • Proficient with Microsoft Office Suite • Advanced level expertise for MS WORD features and macro relation functionalities • Excellent written and oral communication skills • Excellent presentation skills • Strong organizational, problem-solving, and analytical skills • Ability to manage priorities and workflow • Versatility, flexibility, and a willingness to work within constantly changing priorities • Proven ability to handle multiple projects and meet deadlines • Strong interpersonal skills. • Creative, flexible, and innovative team player. • Good judgment with the ability to make timely and sound decisions.
• Competitive salary • Flexible working hours • Professional development opportunities • Remote work options
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