Remote Jobs at Abata Therapeutics

Candidates should possess a Bachelor's or Master's degree in computer science, data science, engineering, or a related field, with 0-4 years of experience. Expertise in one or more programming languages such as Python is required, along with experience with web services and application frameworks like Flask or Django. A solid understanding of database concepts and familiarity with SQL is also necessary, as is familiarity with scripting and cheminformatics toolkits like RDKit, OEChem, or Chemaxon…

Candidates should possess a strong background in medical affairs, ideally with a doctoral degree in a relevant scientific discipline such as pharmacy, medicine, or biology, and a minimum of 10 years of experience in the pharmaceutical or biotechnology industry. Experience in clinical development and medical affairs, specifically with Phase II/III programs, is highly desirable. Proven leadership skills and experience leading medical affairs teams are also required, along with a deep understandi…

Candidates should possess a Bachelor’s degree in a relevant field, such as Computer Science, Information Systems, or a related discipline, and ideally have a Master’s degree. They should have a minimum of 8 years of experience in clinical systems, with a strong understanding of clinical trial operations, data management, and regulatory requirements. Experience with Risk Based Monitoring (RBM), Interactive Response Technology (IRT), Clinical Trial Management Systems (CTMS), Electronic Trial Maste…

Candidates should possess a Bachelor’s degree in Computer Science, Information Systems, or a related field, with a minimum of 8 years of experience in Computer System Validation (CSV) within a regulated environment, preferably in the pharmaceutical or biotechnology industry. Strong knowledge of GxP regulations, including 21 CFR Part 11, is essential, along with experience in leading and managing validation projects.

Candidates should possess a Medical Degree (MD or DO) with board certification in Internal Medicine or a related specialty, and a minimum of 8 years of experience in clinical development, with at least 5 years in a leadership role within the pharmaceutical or biotechnology industry. Strong knowledge of clinical trial design, regulatory requirements, and data analysis is essential, along with demonstrated experience in overseeing clinical studies and collaborating with cross-functional teams.

Candidates should possess a Bachelor’s degree in a scientific discipline, such as biology, pharmacy, or a related field, and have at least 7 years of experience in clinical trial management, with a minimum of 3 years specifically within dermatology or immunology. Demonstrated experience managing multiple clinical trials simultaneously is essential, along with a strong understanding of clinical trial regulations and guidelines.

Candidates should possess a Master’s degree in Biostatistics or a related field, with a strong foundation in statistics and clinical methodologies, combining classical techniques with cutting-edge innovations. They should thrive in fast-paced settings, handle competing priorities with ease, and be results-oriented and collaborative.

The Associate Director, Device Development should possess a strong understanding of biologic/device combination product design and development, technology transfer, and cGMP manufacturing oversight. This role requires experience working with external suppliers, manufacturers, and other functional areas within Technical Operations and Quality, ensuring the development and manufacture of high-quality combination products for clinical supply, commercial manufacturing, and regulatory submissions.

Candidates should possess a Bachelor's degree in a related scientific or healthcare field, and a combination of relevant experience is preferred. They must have a strong understanding of clinical trial processes, regulatory compliance (GCP, FDA, ICH), and the ability to lead cross-functional teams. Strong communication and interpersonal skills are also required.

The ideal candidate should possess a Ph.D. in Molecular Biology, Genetics, Pharmacology, or a related field, along with at least two years of industry experience. Familiarity with perturb-seq and single-cell genomics is required, as is the ability to troubleshoot technical issues, adapt to new protocols, and optimize methodologies for performing large-scale pooled screens. Excellent written and verbal communication skills, including a track record of presenting complex scientific results, are al…

Candidates should possess a Medical Degree (MD or DO) with board certification in Internal Medicine or a related specialty, and a minimum of 10 years of experience in clinical drug development, with at least 5 years specifically in pharmacovigilance and safety. Strong knowledge of global regulatory requirements for pharmacovigilance, including those of the FDA, EMA, and other international regulatory agencies is required, along with experience managing pharmacovigilance vendors and leading safet…

The Senior Director, Clinical Contracts Attorney should possess a Juris Doctor degree and be admitted to practice law in at least one U.S. state, with experience in the biotechnology industry and a strong understanding of clinical trial agreements, informed consent forms, and contract research organization agreements. Ideal candidates will have expertise in all legal aspects of clinical trial operations, including healthcare fraud and abuse, pharmacovigilance, product liability, antitrust, and p…

Candidates should possess an advanced degree in life sciences, such as a PhD, PharmD, or a related field, and demonstrate a strong understanding of clinical trial methodologies and regulatory requirements. They should have at least three years of experience in clinical study design, data analysis, data review, and interpretation, along with good written and verbal communication skills.

Candidates must possess a Bachelor's degree in Computer Science, Engineering, or a related field, coupled with over 7 years of industry experience in AI, machine learning, or similar roles, demonstrating a history of successfully implementing and deploying AI models in production. Proficiency in Python and C++, deep expertise in frameworks like PyTorch/Jax, a strong grasp of deep learning fundamentals including neural network architectures, optimization techniques, and evaluation metrics, and ex…

Candidates must possess a Ph.D. in Biostatistics, Statistics, or a related field with at least 7 years of clinical trials experience, or a Master's degree with 10 years of experience. Required qualifications include up-to-date expertise in statistical methodologies for clinical trial design and analysis, the ability to provide statistical leadership to cross-functional teams, knowledge of FDA regulations and ICH guidelines, expertise in CDISC standards (including ADaM requirements), and advanced…