Catalyst Clinical Research
201 - 500 employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Catalyst Clinical Research is a specialized clinical research organization with a focus on oncology and multi-therapeutic functional service provision for the global biotechnology and biopharmaceutical industries. Through their Catalyst Oncology division, they offer full-service oncology clinical research support, tapping into an extensive site network and experienced global teams to aid cancer drug development. Meanwhile, Catalyst Flex provides specialized functional solutions across clinical operations, data management, biostatistics, and medical writing to strengthen and customize clinical trials. As a partner in drug development, Catalyst Clinical Research delivers flexible, customizable solutions to meet the diverse needs of biotech companies, emphasizing efficiency and innovation in research.
Senior Medical Writer, Evidence Analyst
Job not on LinkedIn
🕒 April 9
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Catalyst Clinical Research
201 - 500 employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Catalyst Clinical Research is a specialized clinical research organization with a focus on oncology and multi-therapeutic functional service provision for the global biotechnology and biopharmaceutical industries. Through their Catalyst Oncology division, they offer full-service oncology clinical research support, tapping into an extensive site network and experienced global teams to aid cancer drug development. Meanwhile, Catalyst Flex provides specialized functional solutions across clinical operations, data management, biostatistics, and medical writing to strengthen and customize clinical trials. As a partner in drug development, Catalyst Clinical Research delivers flexible, customizable solutions to meet the diverse needs of biotech companies, emphasizing efficiency and innovation in research.
📋 Description
• Author, review regulatory & other medical writing deliverables independently or with other Sr Medical Writer • Support other writers for manuscripts, slide sets, abstracts, posters, other techno-commercial documents as needed • Authoring & review of patient narratives, CSRs, Protocol, IB, & other regulatory submission documents • Independent authoring and review of manuscripts, abstracts, posters, evidence synthesis projects and other techno-commercial documents • Undertake quality control of the aforementioned deliverables • Showcase flexibility in terms of timelines and writing style based on client needs and therapeutic area requirements across various domains.
🎯 Requirements
• PharmD, M. Pharm, PhD, MD, Post-graduate degree in Life science/medical/para medical • At least 3-5 years of experience in medical writing or flair for writing with proven academic standards • Fair understanding of industry standards and global trends in drug development and medical device domains • Highly proficient in MS Office and other software for authoring and data handling/interpretation • Basic understanding and comfort for use of automation platforms
🏖️ Benefits
• Commitment to excellence and high standards • Creative, flexible, and innovative team player • Good judgement with the ability to make timely and sound decisions
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