Senior Clinical Scientist
Location: San Diego
Posted on: June 23, 2025
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Job Description:
Job Title: Senior Clinical Scientist Location: San Diego, CA
Position type: FLSA: Full time Exempt Department: Finance ID:
Clinical Development 2201-J09886-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
www.aviditybiosciences.com and engage with us on LinkedIn and X .
The Opportunity This position will support efforts in the strategy,
planning, execution, and reporting of clinical trials. Main
responsibilities include supporting the Program Team Lead and
working with the cross-functional team to execute the trials
according to the clinical development plan. This position will be
responsible for the development of clinical protocols, analysis and
interpretation of safety and efficacy data, and will contribute to
the writing of study documents and regulatory submissions. What You
Will Contribute Contribute to the planning and design of clinical
studies in accordance with corporate objectives Provide scientific
support to the clinical team through literature searches,
interpretation of scientific literature, and evaluation of various
technologies to aid in clinical strategic planning, study
implementation, and due diligence activities Contribute to the
clinical oversight and scientific review of clinical trial data
including summarizing, analyzing and interpreting clinical efficacy
and safety data Support Study Medical Monitor in tracking labs and
communicating with site staff Work in close collaboration with
Clinical Operations to ensure translation of the clinical protocol
into operational deliverables, including but not limited to
performing ongoing review and analysis of clinical study data and
preparing/reviewing study plans Contribute to the writing and
revision of clinical documents, such as study protocols, clinical
study reports, informed consent forms, investigator brochures,
annual reports and other materials for regulatory submission and
assure they are informed of pertinent study information Contribute
to key cross-functional and clinical meetings (e.g., clinical study
team meetings, investigator meetings, site initiation visits, ad
hoc meetings or steering committee meetings) What We Seek Advanced
degree in scientific/life-sciences/clinical/nursing field. M.Sc.,
Ph.D. preferred Minimum of 5-8 years of clinical development
experience, technical/operational experience in planning,
executing, reporting and publishing clinical studies within the
pharmaceutical industry. Demonstrated ability to review and
summarize study data, including experience in preparing and
presenting data Broad understanding of functional areas of drug
development, including preclinical, regulatory, pharmacovigilance,
drug supply, data sciences (data management, biostatistics,
programming), and clinical operations (including site selection,
study start-up, study conduct, and finalization). Successful track
record for the ability to interpret, analyze, and present clinical
data, including aggregate data analyses, in order to inform
decision-making and set clinical strategy. Excellent communication
(oral and written), analytical, organizational, and project
management skills Ability to think strategically and creatively,
function independently, deliver on timelines, have strategic
insights and have a detailed knowledge of the activities, and
procedures involved in clinical drug development Experience with
global clinical studies is a plus Prior experience in Rare Disease
or Neuromuscular Therapy is a plus Ability to multi-task well, to
deal well with conflict and obstacles, and to work in a fast-paced
environment What We Will Provide To You ? The base salary range for
this role is $156,750k - $173,250k. 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: 858-401-7900 F: 858-401-7901
Keywords: , Oceanside , Senior Clinical Scientist, Science, Research & Development , San Diego, California