Remote Jobs at Abata Therapeutics

Candidates should possess a Ph.D. in Pharmaceutical Sciences, Chemistry, Biology, or a related scientific field, with at least 10 years of experience in protein drug product development, including formulation development, process development, aseptic manufacturing, and support of clinical studies. Strong knowledge of regulatory requirements and quality systems, particularly as they relate to biologics, is essential, along with experience in collaborating with cross-functional teams and external …

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 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…

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…

Candidates must possess a Medical Doctorate (M.D.) degree or equivalent, with preferred therapeutic experience in Neurology/Psychiatry. A minimum of 10 years of Pharmacovigilance experience is required, including at least 5 years in a leadership or management role. Strong clinical judgment, organizational abilities, high credibility, significant leadership potential, and experience supervising drug safety processes from development to implementation are essential. Knowledge of regulatory agencie…

Candidates must possess a Bachelor's or Master's degree in Computer Science, Statistics, Mathematics, or a related field. Strong proficiency in SAS programming is required, with experience in R or Python being a plus. In-depth knowledge of CDISC standards (SDTM and ADaM), FDA/EMA regulatory requirements, and ICH guidelines is essential. Experience with eCTD submission programming and contributing to BLA/NDA/MAA filings is preferred. Strong attention to detail, excellent organizational and commun…

Candidates must possess a Ph.D. or M.S. in Biostatistics, Statistics, or a related field, with prior experience in the Biotech/Pharma Industry or a CRO. Required experience includes leading statistical activities for clinical trials across multiple phases, expertise in clinical trial methodology, adaptive designs, and regulatory guidance. Proficiency in SAS, including data simulation and analysis, familiarity with CDISC standards (SDTM/ADaM), and experience with regulatory submissions (NDA/BLA/M…

Candidates must possess an MD degree and at least 15 years of experience in pharmacovigilance. A strong understanding of global regulatory requirements, including FDA, EMA, MHRA, and PMDA, is essential. Experience in leading drug safety strategy and operations, as well as managing pharmacovigilance teams, is required.

Candidates should possess a Bachelor's degree and 10 years of experience, or a Master's degree and 8 years of experience in life sciences, pharmaceutical sciences, or pharmacology. A strong background in conducting clinical pharmacology studies, including study design, PKPD data analysis, and interpretation of results, is essential. A PhD in Pharmaceutical Science or a related discipline is preferred, along with strong quantitative experience such as pharmacometrics.

Candidates should possess a Bachelor's degree in Life Sciences, Information Systems, Engineering, or a related field, or equivalent professional experience. A minimum of 5 years of experience supporting IT systems or business processes within a biotech, pharmaceutical, or regulated life science environment is required, along with direct hands-on experience implementing technical solutions such as workflows and reports.