Job summary
Job post source
This job is directly from Avidity Biosciences, Inc.
Job overview
The Associate Director, Medical Writing at Avidity Biosciences will oversee medical writing deliverables and collaborate with cross-functional teams to enhance the development of RNA therapeutics.
Responsibilities and impact
The role involves managing the development and review of medical documents, coordinating with stakeholders, ensuring compliance with regulatory standards, and providing training on writing processes.
Compensation and benefits
The base salary range is $176,600 to $195,200, with additional benefits including bonuses, stock options, a 401(k) match, and comprehensive wellness coverage.
Experience and skills
Candidates should have a PhD or Master's in life sciences, 7+ years of relevant experience, and extensive knowledge of medical writing best practices and regulatory submissions.
Career development
Avidity offers learning and development opportunities, including job-specific training and an education reimbursement program.
Work environment and culture
The company promotes a collaborative and agile culture focused on patient needs and values transparency and accountability.
Company information
Avidity Biosciences specializes in RNA therapeutics, particularly Antibody Oligonucleotide Conjugates (AOCs), and is based in San Diego, CA, with a focus on innovative treatments for rare muscle diseases.
Team overview
The candidate will work within a high-functioning matrixed team, reporting to the Director of Medical Writing.
Job location and travel
The position is based in San Diego, CA, with hybrid and remote work options available.
Unique job features
The role offers the opportunity to lead critical document development and engage in innovative projects within a growing pipeline.
Company overview
Avidity Biosciences is a biopharmaceutical company specializing in the development of antibody-oligonucleotide conjugates (AOCs) aimed at treating serious diseases. They generate revenue primarily through strategic partnerships, licensing agreements, and the development of proprietary therapies. Founded in 2012, Avidity has made significant strides in advancing its AOC platform, which combines the precision of monoclonal antibodies with the therapeutic potential of oligonucleotides, positioning itself as a leader in the field of targeted genetic medicine.
How to land this job
Position your resume to highlight your extensive experience in medical writing, particularly in clinical protocols and clinical study reports, as these are key responsibilities for the Associate Director role at Avidity Biosciences, Inc.
Emphasize your project management skills and ability to collaborate with cross-functional teams, showcasing any experience with regulatory submissions and document development that aligns with the job description.
Apply through multiple channels, including Avidity Biosciences' corporate site and LinkedIn, to maximize your visibility and chances of landing the position.
Connect with professionals in the Regulatory Affairs division at Avidity Biosciences on LinkedIn, and consider ice breakers like expressing your enthusiasm for their innovative RNA therapeutics or asking about their experiences with the AOC platform.
Optimize your resume for ATS systems by incorporating specific keywords from the job description such as 'medical writing', 'clinical study reports', and 'regulatory submissions' to enhance your chances of passing initial screenings.
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