Senior Clinical Scientist
Senior Clinical Scientist
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Job Description
Description
Job Title:
Senior Clinical Scientist
Location:
San Diego CA
Position type:
FLSA:
Full time
Exempt
Department:
Finance ID:
Clinical Development
2201J09886BF
Profoundly Improve Peoples 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 peoples 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 solutionoriented 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 peoples lives by delivering a new class of RNA therapeutics Antibody Oligonucleotide Conjugates (AOCs). Utilizing its proprietary AOC platform Avidity demonstrated the firstever 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 inSan 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
This positionwill support efforts in the strategy planningexecutionand reporting of clinical responsibilities include supporting theProgram Team Leadand working with the crossfunctional team to execute the trialsaccording to the clinical development plan. This position will be responsible forthe development of clinical protocolsanalysis and interpretation of safety and efficacy data and will contribute to the writing ofstudy 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 andscientificreview 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 crossfunctional 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/lifesciences/clinical/nursing field. . Ph.D. preferred
- Minimum of58years of clinical development experiencetechnical/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 startup 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 decisionmaking 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
- Priorexperience in Rare DiseaseorNeuromuscular Therapy is a plus
- Ability to multitask well to deal well with conflict and obstacles and to work in a fastpaced environment
What We Will Provide To You
The base salary range for this role is $156750k $173250k. 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 jobspecific training offered by industry and an education reimbursement program.
Avidity Biosciences
10578 Science Center Dr. Suite 125
San Diego CA
92121
O:
F:
Required Experience:
Senior IC
Employment Type
Full-Time
