Research Associate I, Translational Biology
Sarepta Therapeutics
Date: 1 week ago
City: Columbus, OH
Salary:
$57,200
-
$71,500
per year
Contract type: Full time
Why Sarepta? Why Now?
The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more than 40 programs in various stages of development in gene therapy, RNA and gene editing. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne.
We’re looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients.
What Sarepta Offers
At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resources designed to support people in the following areas:
The Importance of the Role
Sarepta Therapeutics is seeking a motivated individual to conduct activities in the Translational Biology Department. The qualified candidate will provide laboratory support of day-to-day GCLP/GLP testing of molecular and histological based methods in accordance with the requirements of approved protocols; maintain records of experiments; assist in analyzing data and prepare laboratory reports; perform necropsy and biological sample processing. This person may participate in development, GCLP/GLP qualification, and validation of assays to support clinical trials and clinical development decision-making.
The Opportunity to Make a Difference
We’re always looking for solution-oriented, critical thinkers.
So, if you’re comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply.
This position requires work on site at one of Sarepta’s facilities in the United States.
The targeted salary range for this position is $57,200 - $71,500 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta’s compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity.
Candidates must be authorized to work in the U.S.
Sarepta Therapeutics offers a competitive compensation and benefit package.
Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.
The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more than 40 programs in various stages of development in gene therapy, RNA and gene editing. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne.
We’re looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients.
What Sarepta Offers
At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resources designed to support people in the following areas:
- Physical and Emotional Wellness
- Financial Wellness
- Support for Caregivers
The Importance of the Role
Sarepta Therapeutics is seeking a motivated individual to conduct activities in the Translational Biology Department. The qualified candidate will provide laboratory support of day-to-day GCLP/GLP testing of molecular and histological based methods in accordance with the requirements of approved protocols; maintain records of experiments; assist in analyzing data and prepare laboratory reports; perform necropsy and biological sample processing. This person may participate in development, GCLP/GLP qualification, and validation of assays to support clinical trials and clinical development decision-making.
The Opportunity to Make a Difference
- Assist in the execution of GCLP/GLP clinical sample processing and testing using a variety of molecular formats including ELISA, western blot and ddPCR.
- Support the development of molecular assays to prepare for method validation studies.
- Assist in the execution of GCLP/GLP clinical and non-clinical study sample preservation and processing.
- Assist in the execution of GLP non-clinical sample processing and testing using a variety of molecular formats including ELISA, western blot and ddPCR.
- Performs protocol specific necropsy evaluations of laboratory animals, including but not limited to sample container preparation, harvesting, and weighing of tissues and accurate and timely record keeping.
- Processes tissue, blood, urine, and other samples as needed.
- Handling, organizing, and tracking study samples in the laboratory and coordinating with Research Operations.
- Maintaining summary tables and trackers for internal and bioanalytical reports.
- Additional duties include completing general lab tasks, preventive maintenance and quality control. Maintaining a clean working area and adheres to proper safety techniques and procedures. Performs miscellaneous related duties as required.
- Ensure compliance with GCP/GLP documentation guidelines.
- Additional duties as assigned.
- B.A. or B.S. degree in Biochemistry, Immunology, Cell Biology, Molecular Biology, Genetics or related field with 1-3 years of relevant experience in a laboratory setting.
- Ability to execute sample handling and analysis with strict adherence to laboratory methods and SOPs.
- Experience with computer productivity software (i.e. Microsoft Word, Excel, etc.).
- Knowledge of routine molecular procedures.
- Strong problem solving and data analysis skills.
- Ability to plan and carry out experiments independently with strict adherence to laboratory methods and SOPs.
- Experience and/or willingness to be trained in necropsy procedures.
- Desire to work in a high-functioning, collaborative team across multiple therapeutic platforms.
- Desire to work in a dynamic, fast-paced team environment and to make a difference in the lives of people through our innovative medicines.
We’re always looking for solution-oriented, critical thinkers.
So, if you’re comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply.
This position requires work on site at one of Sarepta’s facilities in the United States.
The targeted salary range for this position is $57,200 - $71,500 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta’s compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity.
Candidates must be authorized to work in the U.S.
Sarepta Therapeutics offers a competitive compensation and benefit package.
Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.
How to apply
To apply for this job you need to authorize on our website. If you don't have an account yet, please register.
Post a resumeSimilar jobs
Pharmacy Patient Asstnce Coord (HS)
The Ohio State University Wexner Medical Center,
Columbus, OH
1 week ago
Scope of Position
The Ohio State University Medical Center is committed to improving access and service to customers. The Medication Assistance Program Coordinator (MAPC) functions as an integral member of the health care team to reflect a culture of cooperation, enthusiasm and mutual respect. This position coordinates patient access to medications necessary for their treatment, regardless of their ability to...
Territory Sales Representative
Phathom Pharmaceuticals,
Columbus, OH
3 weeks ago
DescriptionPhathom Pharmaceuticals is a biopharmaceutical company focused on the development and commercialization of novel treatments for gastrointestinal (GI) diseases. We have licensed the exclusive rights in the United States, Europe, and Canada to vonoprazan, a first-in-class potassium-competitive acid blocker (PCAB). Phathom currently markets VOQUEZNA (vonoprazan) tablets for the treatment of heartburn associated with Non-Erosive GERD in adults, the healing and...
Project Coordinator
Abbott,
Columbus, OH
4 weeks ago
Title: Project CoordinatorLocation: Columbus, OhioDuration: 12 MonthsJob DescriptionThis person will support project / program managers across the global project portfolio by being responsible for:Setup of new projects / programs including laying out the initial project plan based on approved project requests. This will include working within the project / portfolio management system to ensure project details, milestones, and resources are...