Avidity Biosciences, Inc.
Manager, Regulatory Affairs
Avidity Biosciences, Inc., San Diego, California, United States, 92189
Job Title:Manager
, Regulatory AffairsLocation:San Diego
, CA / Hybrid / RemotePosition type:FLSA:Full timeExemptDepartment
:Finance ID:Regulatory and Quality8300-Q224-4Strive to Bring a
Profound Difference to our Patients
At Avidity Biosciences, we are passionate about the impact of every employee in realizing our vision of improving people’s lives by delivering a new class of RNA therapeutics.
Avidity is revolutionizing the field of RNA with its proprietary AOCs, which are designed to combine the specificity of monoclonal antibodies with the precision of oligonucleotide therapies to address targets and diseases previously unreachable with existing RNA therapies.
If you are a committed, solution-oriented thinker, join us in making a difference and become part of our growing culture that is integrated, collaborative, agile and focused on the needs of patients.Avidity Biosciences, Inc.'s mission is to profoundly improve people's lives by delivering a new class of RNA therapeutics - Antibody Oligonucleotide Conjugates (AOCs). Utilizing its proprietary AOC platform, Avidity demonstrated the first-ever successful targeted delivery of RNA into muscle and is leading the field with clinical development programs for three rare muscle diseases: myotonic dystrophy type 1 (DM1), Duchenne muscular dystrophy (DMD) and facioscapulohumeral muscular dystrophy (FSHD). Avidity is broadening the reach of AOCs with its advancing and expanding pipeline, including programs in cardiology and immunology through internal discovery efforts and key partnerships. Avidity is headquartered in
San Diego, CA.
For more information about our AOC platform, clinical development pipeline, and people, please visit
www.aviditybiosciences.com
and engage with us on
LinkedIn
and
Twitter
.The OpportunityReporting to
an Associate Director, CMC Regulatory Affairs,
the successful candidate will work independently and collaborate cross
‐
functionally to provide guidance to the CMC subject matter experts and manage and execute CMC regulatory submissions to facilitate the global development of Avidity compounds.What You Will ContributeManag
e
preparation, drafting, and review of CMC
content regulatory submissions (e.g. INDs, IMPDs, BLAs) to ensure timelines are metWork collaboratively with CMC subject matter experts and external partners
to track source documentation and allow for
successful complet
ion of
CMC regulatory submissionsPartner with stakeholders to identify, manage, escalate, and resolve issues related to optimal team performanceSupport
responses to Health Authority inquiriesSupport preparation for and management of CMC interactions with Health AuthoritiesContribute to the development of CMC strateg
ies and solutions within program teamsEnsure compliance with quality assurance and regulatory procedure and work practiceContribute to ongoing process improvement and department initiatives within the CMC Regulatory Affairs function, including process improvements, SOP review and development, development of training, etc.Effectively collaborate in a highly matrixed organizationWhat We See
kBachelor’s Degree, at a minimum, (advanced degree preferred) in life sciences or chemistry, with a minimum of
3 - 5
years of experience in Regulatory Affairs with a CMC focus within a biotechnology company
and/or 5
+
years of experience within biopharmaceutical
technical operations
or equivalent combination of education and experienceEstablished working knowledge of regulatory guidelines and regulations, US and internationalStrong eCTD knowledge and regulatory writing skillsSelf
‐
motivated, self
‐
disciplined, and able to function independently as well as part of a teamStrong organizational skills and ability to maintain a high level of communication, productivity, innovation, and priority
‐
setting to work effectively in a dynamic environment to meet aggressive timelinesStrategic agility, strong critical and logical thinking with the ability to analyze and propose solutions to problemsExcellent computer proficiency (MS Word, Excel, PowerPoint, Adobe Acrobat)Ability to travel as neededWhat We will Provide to You:
The base salary range for this role is
$135,100
to
$149,300
.
The final compensation
will be commensurate with such
factors
as
relevant experience, skillset, internal equity and market factors
.Avidity offers competitive compensation and benefits which includes the opportunity for annual and spot bonuses, stock options and RSUs, as well as a 401(k) with an employer match. In addition, the comprehensive wellness program includes coverage for medical, dental, vision, and LTD, and four weeks of time off.A commitment to learning and development which includes a variety of programming internally developed by and for Avidity employees, opportunities for job-specific training offered by industry, and an education reimbursement program.Avidity Biosciences10578 Science Center Dr. Suite 125San Diego, CA92121O: 858-401-7900F: 858-401-7901
#J-18808-Ljbffr
, Regulatory AffairsLocation:San Diego
, CA / Hybrid / RemotePosition type:FLSA:Full timeExemptDepartment
:Finance ID:Regulatory and Quality8300-Q224-4Strive to Bring a
Profound Difference to our Patients
At Avidity Biosciences, we are passionate about the impact of every employee in realizing our vision of improving people’s lives by delivering a new class of RNA therapeutics.
Avidity is revolutionizing the field of RNA with its proprietary AOCs, which are designed to combine the specificity of monoclonal antibodies with the precision of oligonucleotide therapies to address targets and diseases previously unreachable with existing RNA therapies.
If you are a committed, solution-oriented thinker, join us in making a difference and become part of our growing culture that is integrated, collaborative, agile and focused on the needs of patients.Avidity Biosciences, Inc.'s mission is to profoundly improve people's lives by delivering a new class of RNA therapeutics - Antibody Oligonucleotide Conjugates (AOCs). Utilizing its proprietary AOC platform, Avidity demonstrated the first-ever successful targeted delivery of RNA into muscle and is leading the field with clinical development programs for three rare muscle diseases: myotonic dystrophy type 1 (DM1), Duchenne muscular dystrophy (DMD) and facioscapulohumeral muscular dystrophy (FSHD). Avidity is broadening the reach of AOCs with its advancing and expanding pipeline, including programs in cardiology and immunology through internal discovery efforts and key partnerships. Avidity is headquartered in
San Diego, CA.
For more information about our AOC platform, clinical development pipeline, and people, please visit
www.aviditybiosciences.com
and engage with us on
and
.The OpportunityReporting to
an Associate Director, CMC Regulatory Affairs,
the successful candidate will work independently and collaborate cross
‐
functionally to provide guidance to the CMC subject matter experts and manage and execute CMC regulatory submissions to facilitate the global development of Avidity compounds.What You Will ContributeManag
e
preparation, drafting, and review of CMC
content regulatory submissions (e.g. INDs, IMPDs, BLAs) to ensure timelines are metWork collaboratively with CMC subject matter experts and external partners
to track source documentation and allow for
successful complet
ion of
CMC regulatory submissionsPartner with stakeholders to identify, manage, escalate, and resolve issues related to optimal team performanceSupport
responses to Health Authority inquiriesSupport preparation for and management of CMC interactions with Health AuthoritiesContribute to the development of CMC strateg
ies and solutions within program teamsEnsure compliance with quality assurance and regulatory procedure and work practiceContribute to ongoing process improvement and department initiatives within the CMC Regulatory Affairs function, including process improvements, SOP review and development, development of training, etc.Effectively collaborate in a highly matrixed organizationWhat We See
kBachelor’s Degree, at a minimum, (advanced degree preferred) in life sciences or chemistry, with a minimum of
3 - 5
years of experience in Regulatory Affairs with a CMC focus within a biotechnology company
and/or 5
+
years of experience within biopharmaceutical
technical operations
or equivalent combination of education and experienceEstablished working knowledge of regulatory guidelines and regulations, US and internationalStrong eCTD knowledge and regulatory writing skillsSelf
‐
motivated, self
‐
disciplined, and able to function independently as well as part of a teamStrong organizational skills and ability to maintain a high level of communication, productivity, innovation, and priority
‐
setting to work effectively in a dynamic environment to meet aggressive timelinesStrategic agility, strong critical and logical thinking with the ability to analyze and propose solutions to problemsExcellent computer proficiency (MS Word, Excel, PowerPoint, Adobe Acrobat)Ability to travel as neededWhat We will Provide to You:
The base salary range for this role is
$135,100
to
$149,300
.
The final compensation
will be commensurate with such
factors
as
relevant experience, skillset, internal equity and market factors
.Avidity offers competitive compensation and benefits which includes the opportunity for annual and spot bonuses, stock options and RSUs, as well as a 401(k) with an employer match. In addition, the comprehensive wellness program includes coverage for medical, dental, vision, and LTD, and four weeks of time off.A commitment to learning and development which includes a variety of programming internally developed by and for Avidity employees, opportunities for job-specific training offered by industry, and an education reimbursement program.Avidity Biosciences10578 Science Center Dr. Suite 125San Diego, CA92121O: 858-401-7900F: 858-401-7901
#J-18808-Ljbffr