Job Title:
Executive Director, Clinical Supply Chain
Location:
Hybrid
Position type:
FLSA:
Full time
Exempt
Department:
Finance ID:
TD&O
7625-Q224-29
Strive 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 and engage with us on LinkedIn and Twitter .
The Opportunity
We are seeking an Executive Director, Clinical Supply Chain, who is experienced in building and managing clinical supply teams and is a senior leader accountable for developing and executing Avidity's clinical supply strategy. The individual will report to the Vice President, Global Supply Chain and be accountable to manage supply across all of Avidity's clinical programs. As Avidity expands and strengthens its global supply network, our team and systems will expand accordingly. Overall responsibility will include clinical demand and supply planning, vendor forecast management, IRT support and ownership of labeling, kitting, and clinical distribution operations. A strong knowledge of cGMP and global clinical supply requirements is required.
What You Will ContributeLead Avidity's clinical supplies team including support of existing team member career development, recruitment of new members and development of Clinical Supply organizational structureProvide strategic leadership for all of Avidity's clinical programs, including demand/supply/capacity planning, label development (including translations), global labeling strategy, packaging and kitting operations, inventory management and support for cold chain shipments as needed (i.e. temperature excursions).Partner with Executive Director, Commercial Supply Chain to strengthen clinical supply forecast models to feed into Avidity's S&OP process.Manage implementation of Avidity's clinical forecasting tool.Provide strategic and operational ownership of all clinical packaging sites, monitor site performance with business reviews and KPIs and provide leadership for expansion of CRO vendor network.Ensure clinical drug inventory levels are maintained in accordance with study plans and that inventory is strategically positioned in accordance with enrolment projections.Provide support for Avidity's pharmacy manuals and investigator brochures, as required.Strengthen procedural elements of the clinical supply team including review, development and maintenance of Clinical Supply SOPs.Ensure accurate and timely communication to Program teams of any clinical supply risks. Work cross-functionally to strategically manage clinical inventory in accordance with manufacturing schedules and regulatory submission/approvals.Provide support for regulatory filings IND, CTA, and IMPD updates as needed. Respond to RFIs in a timely manner in partnership with Regulatory.Develop appropriate regional labeling strategy to make optimal use of limited clinical inventory.Monitor pharmaceutical preparation and dose administration questions from clinical investigator sites and develop Avidity's response strategy.Assist in pull-forward of Avidity's clinical/site experience to newly forming commercial and medical teams preparing for launch.Ensure adherence to applicable regulations including FDA, EMA, ICH, GCP, GMP and Avidity policies and procedures. Support Avidity QMS and RIMS systems as needed. What We Seek
Bachelor's Degree in pharmaceutical sciences, chemistry, biology, engineering or related field is required; Advanced Degree preferred.
A minimum of 12 years of Clinical Supply management with 12 years' experience managing and developing direct reports.
Experience working with third-party CMOs manufacturing cGMP clinical supplies (labeling, kitting, clinical supply serialization, etc).
Experience with dose calculations for weight-based infusions.
Experience supplying clinical product to US, Canada, UK, EU, APAC and LATAM.
Experience with Excel at a minimum. Experience with external clinical forecasting systems (i.e. Signant Health or other) is a plus.
Knowledge of IRT system sourcing, development, and use. Ability to support IRT user acceptance testing as well as required updates to system for implementation of study protocol changes.
Knowledge of cGMP, ICH, FDA, EMA guidelines regarding temperature controlled cold chain shipping requirements. Ability to coordinate requirements with Avidity's shipping & logistics team.
Proven track record of effective collaboration with external providers.
Excellent communication and interpersonal skills and the ability to facilitate constructive, expedient problem-solving.
Ability to travel as needed.
What We Will Provide to You: The base salary range for this role is $270,750 - $300,000. The final compensation will be commensurate with such factors as relevant experience, skillset, internal equity and market factors.
Avidity offers competitive compensation and benefits, including 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, including a variety of internal programming developed by and for Avidity employees, opportunities for job-specific training offered by industry, and an education reimbursement program.
Avidity Biosciences
10578 Science Center Dr. Suite 125
San Diego, CA
92121
O:
F:
Job Title:
Manager, Quality Control Stability
Location:
Hybrid - San Diego and Remote
Position type:
FLSA:
Full time
Exempt
Department:
Finance ID #:
CMC/Technical Operations
3101-J45358-BF
Company Overview At Avidity Biosciences, we are passionate about the impact of every employee in bringing potentially life-changing therapeutics to patients in need. Avidity is pioneering a new class of oligonucleotide-based therapies called AOCs designed to overcome the current limitations of oligonucleotide therapies to treat a wide range of serious diseases. We utilize our proprietary AOC platform to design, engineer and develop transformative therapeutics that combine the tissue selectivity of monoclonal antibodies (mAbs) and the precision of oligonucleotide-based therapies to access previously undruggable tissue and cell types and more effectively target underlying genetic drivers of diseases. If you are a committed, solution-oriented thinker, come make a difference with us.
Position Overview
The Manager, Quality Control Stability will lead QC activities associated with the day-to-day coordination and execution of the stability program at Avidity. This position will oversee stability data generated at CMOs/CROs relating to the GMP testing of Avidity's products including drug substance intermediates, drug substance and drug product. This individual will provide input to cross-functional teams and ensure effective communication with colleagues and external partners. Excellent verbal and written communication skills are essential for success in this position including extensive experience successfully managing multiple CTOs and CMOs. This position will report to the Sr. Manager, QC Stability and be a part of Avidity's CMC / Technical Operations team.
ResponsibilitiesManage and oversee the stability program and QC testing in accordance with Avidity procedures and regulatory guidelines. Support cGMP operations and technical review of both internal and external (CMO) records, including stability test records/reports, protocols, change controls, deviations, and OOS. Provide technical review for stability data from various assays across multiple product types, including mAb, oligonucleotide, and DS/DP AOCs. Assess, analyze, and trend stability data.Author shelf-life justification reports.Support oversight of QC activities at CMOs including SOW review, data quality, and adherence to timelines. Communicate data both verbally at group meetings, CMC teams, and through written documents and reports. Assist in the preparation of CMC regulatory submissions. Write and revise standard operating procedures. Work with project leads to address delays and escalate when necessary. Support other QC activities and projects as needed.This position may require travel (approximately 10%). Qualifications
The ideal candidate for this position will have extensive QC experience in a cGMP biologics regulated manufacturing environment is required. The role will interface with Quality Assurance, Supply Chain, Manufacturing, Analytical Development, and Regulatory groups to ensure company procedures and industry guidelines are followed. The candidate will possess a strong technical background, and proven track record in Quality Control related to biologics, oligonucleotides, and AOC (Antibody Oligonucleotide Conjugate)/ADC modalities.BS or MS in a Chemistry, Biochemistry, Microbiology, Biology, or other related field5+ years of related experience within the biopharmaceutical industry in QC management, with a focus on QC StabilityWorking knowledge of antibody, antibody drug conjugates, oligonucleotides and protein analytical methods is strongly preferred.Demonstrated knowledge of cGMP/ICH/FDA/EU/PMDA regulationsDemonstrated knowledge of USP, EP, and JP monographsHighly collaborative team player who fosters open communication and facilitates mutual understanding and cooperation between all stakeholdersA passion for addressing the critical unmet medical needs of patientsSelf-directed individual who is able to work with limited direction in a fast-paced, goal-oriented environmentAbility to organize data and identify gapsKnowledge of Good Manufacturing Practices and Good Laboratory Practices. Experience of managing CMO relationships and projectsSound understanding and demonstrated application of statistical methods/toolsExcellent interpersonal skills, outstanding organizational skills, and excellent written and oral communication skills.What We will Provide to You:The base salary range for this role is $142,500 - $157,500. 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 Biosciences
10578 Science Center Dr. Suite 125
San Diego, CA
92121
O:
F:
Job Title:
Administrative Assistant
Location:
San Diego, CA
Position type:
FLSA:
Full Time
Non-Exempt
Department:
R&D Admin
Profoundly Improve People's lives by Revolutionizing the Delivery of RNA Therapeutics
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 and engage with us on LinkedIn and Twitter .
Position Overview The Administrative Assistant will be responsible for performing several administrative duties. This is a pivotal, multi-tasking role that requires strong leadership skills and the ability to think on your feet. The Administrative Assistant must quickly assess situations, find solutions and take decisive action, often under pressure of deadlines and often unpredictable workloads.
What You Will ContributeCoordinate daily schedules, meetings, agendas, presentations, travel arrangements, and expense reports for various team members.Coordinate travel for team members, interview candidates, and key partners.Schedule departmental interviews and assist with recruitment activities.Interact heavily with Purchasing and Legal with regard to contracts management and making purchasing requests.Support and follow through on business financial transactions (purchase requests, invoice approvals).Act as a liaison among functional groups, internal and external contacts.Prioritize and direct incoming business matters in a timely and efficient manner.Work collaboratively with other executive and administrative assistants.Develop documents, presentations, graphs, and charts for various routine to complex ad-hoc projects using word processing, spreadsheet, and graphics software.Support on-site activities such as department meetings and company-wide events.Coordinate on-site lunches for meetings and off-site dinners.Provide back-up support to the office coordinator and assist with office coordination and facilities management.Proactively identify and solve problems to ensure smooth operations.Must work at the office Monday - Friday unless otherwise directed.Complete and manage projects as assigned.Perform other duties as required.What We SeekEducation and ExperienceMinimum 3-5 years of experience as an administrative assistant, office manager or other applicable roles Desired Knowledge and AbilitiesExperience working with professionalism and discretion.Outstanding communication, organizational, and interpersonal skills; strong customer service orientation.Strong organizational skills with the ability to multi-task and meet deadlines.Attention to detail and excellent problem-solving skills.Ability to prioritize tasks and manage time effectively.Proactive in managing tasks and workloads; flexible and able to adapt/adjust with short notice.Capable of making good judgments, anticipating needs, and working independently.Maintain positive, professional relationships with personnel at all levels of the organization.Expert knowledge and proficiency with Microsoft O365 suite and Zoom.Proficiency with Concur or travel and expense systemPrevious biotech/pharma work experience preferred. What We will Provide to You: The base salary range for this role is $71,250 to $78,750 ($34 to $38/hour). The final compensation will be commensurate with such factors as relevant experience, skillset, internal equity and market factors. Avidity Biosciences
10578 Science Center Dr. Suite 125
San Diego, CA
92121
O:
F:
Job Title:
Director, Biostatistics
Location:
San Diego, CA / Hybrid / Remote
Position type:
FLSA:
Full time
Exempt
Department:
Finance ID:
Biometrics
-4-P
Strive 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 and engage with us on LinkedIn and Twitter .
The Opportunity
The Director of Biostatistics will serve as a program statistical lead and may lead one or more studies. The position will provide technical leadership and biostatistical support for clinical trial design, conduct, evaluation, and interpretation of study results. This position will also involve regulatory responses and filing activities, contributing to statistical analyses, and preparing the submission data package.
Additionally, the position will be involved in department or cross-functional departmental standards, processes, training, and initiatives.
What You Will ContributeServe as a lead statistician for a pivotal study or at the program level. Provide statistical support to cross-functional teams. Provide input into product development strategy and decision-making (e.g., considerations for interim analyses, innovative designs, comparisons with natural history studies or competitors, etc.)Contribute to research in advanced statistical methodologiesLead/support the regulatory interaction and submission activitiesReview CRFs and other study documentation and draft statistical analysis plan (including ISS/ISE) and develop TFL shell and specificationManage CRO and oversee the execution of statistical analyses, review statistical outputsCreate/review study randomization files and contribute to the protocol, IDMC charter, and study-related document authoringPresent and interpret study results and author and review regulatory documents (including CSR) and publications. Work with the biometrics team to provide the data package relevant for submission or reimbursement. Contribute to developing department standards, procedures, and initiativesMentor junior statisticians and summer interns What We SeekGenerally PhD in Biostatistics or Statistics with 10+ years (or MS with 12+ years) of relevant pharmaceutical experienceExperienced in leading an indication and phase 3 studies independently Experienced in NDA / BLA / MAA activities as a key contributor from a statistics perspective and direct involvement in regulatory interactionStrong background and working knowledge of statistical methods that apply to all phases of clinical trials and other study designs.Experienced in hands-on study-level work including authoring SAP, TFL specification, and validating outputsKnowledge of CDISC including SDTM, ADaM, and controlled terminologies Have a working knowledge of all appropriate relevant regulatory guidance documents (e.g. ICH, FDA, and EMEA)Ability to respond to regulator's inquiries for products undergoing registration and approved productsDemonstrated organized, detail-oriented, and problem-solving skills and ability to prioritize and complete multiple tasks to meet the timeline. Flexible to adapt to change.Strong communication and interpersonal skills, with the ability to work collaboratively in a team environment.Familiar with SAS and other statistical software (i.e. R, Python, etc.)The preferred candidate will also have career experience working in rare disease, experience with using statistical methods to analyze longitudinal data, and advanced statistical knowledge such as adaptive design, real-world data comparison, machine learning, and AI applications. What We Will Provide To You
The base salary range for this role is $232,750 - $257,250. 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 include 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 Biosciences
10578 Science Center Dr. Suite 125
San Diego, CA
92121
O:
F:
Job Title:
Senior Research Associate, in vivo Biology
Location:
San Diego, CA
Position type:
FLSA:
Full time
Non-Exempt
Department:
Finance ID:
Biology
1201-R55492-BF
Profoundly Improve People's Lives by Revolutionizing the Delivery of RNA Therapeutics
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 and engage with us on LinkedIn and X .
The Opportunity
We are seeking an experienced in vivo Biology Research Associate to characterize in vivo properties of novel therapeutic Antibody Oligonucleotide Conjugates that deliver nucleic acids. The candidate will be part of a small team responsible for executing in vivo animal studies across multiple projects, including PK, PD, and biomarker analyses. Prior experience with rodent handling, multiple dosing routes, blood collection, and tissue sample collection is required. The associate will closely collaborate with colleagues in pre-clinical discovery and present scientific results to multidisciplinary teams and senior management.
What You Will ContributeDrive forward preclinical research projects to expand Avidity's AOC platform through in vivo data.Research and incorporate new techniques, when applicable, to expand in vivo team capabilitiesProvide input on in vivo experimental design across platform projects.Collaborate with team members across multiple departments throughout Avidity to deliver on corporate goals What We SeekB.S./B.A. degree in the biological sciences with at least 2+ years of relevant in vivo animal study experience, preferably in an industry settingProficient in various mouse and rat dosing techniques - IV, SC, IP, RO, ICV, ITH. Must have high proficiency in IV dose administration in C57BlL/6 background mice.Proficient in survival and terminal bleeding techniques - RO, Tail, Submental, Cardiac.Demonstrate proper handling of biological samples and protein biologics Knowledge of laboratory rodent behavior, anatomy, and guiding principles for animal welfareSurgical and/or micro-dissection experience preferredStrong organizational skills and attention to detail, including the ability to manage several projects simultaneously. Proficient computer and data collection/analysis skills - Microsoft Office Suite, Prism, Benchling preferredAbility to work and troubleshoot independently and in a team setting. Physical Requirements/DemandsRepetitive motions that may include the fingers, wrists, hands, and/or legsRemaining in a stationary position, often standing or sitting for prolonged periodsAdjusting or moving objects up to 50 pounds.Operating machinery and laboratory equipmentExposure to animal allergens Environmental ConditionsLow and Vivarium temperaturesNoisy environmentsExposure to general laboratory and vivarium environment conditions.Exposure to general office environment conditions. What We Will Provide To YouThe base salary range for this role is $40/hr. - $45/hr. The final compensation will be commensurate with relevant experience, skillset, internal equity, and market factors.Avidity offers competitive compensation and benefits, including 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, including a variety of internal programming developed by and for Avidity employees, opportunities for job-specific training offered by industry, and an education reimbursement program. Avidity Biosciences
10578 Science Center Dr. Suite 125
San Diego, CA
92121
O:
F:
Job Title:
Staff Accountant
Location:
Hybrid
Position type:
FLSA:
Full time
Exempt
Department:
Finance ID:
Accounting
-1
Profoundly Improve People's lives by Revolutionizing the Delivery of RNA Therapeutics
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 and engage with us on LinkedIn and X .
The Opportunity
The Staff Accountant is an important part of the accounting team and will support a diverse range of subjects across multiple business process cycles. The ideal candidate possesses a positive attitude, is self-motivated, and eager to learn new things while having an impact across a broad scope of areas at the Company. Further, the ideal candidate will have a focus on optimizing processes to be more scalable and efficient in preparation for future growth and globalization of the Company.
What You Will ContributePrepares recurring journal entries, reconciliations, and accounting analysis applicable to the groupLearns and maintains standard practices of the departmentDevelops and maintains process documentationIntegrate with other functions to the extent needed to optimize key process and ensure scalable growthHas a customer service mindset when working with other groupsIntellectually curious and drive to understand the "why" behind each process and proceduresAbility to think outside the box and develop new processes and process improvementsA relentless approach to learning with the ability to make connections among previously unrelated notions and come up with a lot of new and unique ideasAbility to develop a strong understanding of the holistic Avidity business and processes to help build and prepare for long-term successTypically works autonomously with little instruction on day-to-day workSelf-starter with strong internal driveBuilds cross functional relationshipsWorks autonomously on routine work, and receives coaching on new projects What We Seek Bachelor's Degree in a relevant discipline area and 2+ Years of experience in either an Auditing role or Corporate Accounting Basic knowledge of US GAAP Basic Excel/MS Office & ERP skills Basic workpaper and documentation skills Good organizational skills Preferred BackgroundBig 4 or other Large National Audit Firm experienceCorporate Accounting experience Experience with D365 or other large ERP systems Licensed CPA or in progress with the CPA ExamWhat We will Provide to You:The base salary range for this role is $75,000 - $85,000. 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 Biosciences
10578 Science Center Dr. Suite 125
San Diego, CA
92121
O:
F:
