Clinical Research Associate Salary at Bioagile Therapeutics Pvt Ltd BETA

*** MUST BE LOCAL TO CA OR NY STATE - NO EXCEPTIONS *** Salary: $100K-$130K Company Summary: A global, specialty pharmaceutical group with an impressive track record is seeking a motivated Clinical Research Associate for a hybrid role at their San Francisco site. Their commercial supply of pharmaceutical products generated $83m in revenue in FY2023 (a 24% uptick from the year prior). Since their first clinical trials in 2006, they've had 3 approvals already on the market. Currently, they have 6 indications in Phases II and III, so they are looking for a driven, growth-oriented Clinical Research Associate to facilitate their in house studies. The CRA will be responsible for: Managing and investigating clinical trials and/or post-authorization safety studies Performing and coordinating different aspects of clinical monitoring and site management 20-25% travel (1x a month) An ideal candidate for this role MUST have… 2+ years of ONSITE monitoring experience at a sponsor or CRO (academia do

*** MUST BE LOCAL TO CA OR NY STATE - NO EXCEPTIONS *** Salary: $100K-$130K Company Summary: A global, specialty pharmaceutical group with an impressive track record is seeking a motivated Clinical Research Associate for a hybrid role at their San Francisco site. Their commercial supply of pharmaceutical products generated $83m in revenue in FY2023 (a 24% uptick from the year prior). Since their first clinical trials in 2006, they've had 3 approvals already on the market. Currently, they have 6 indications in Phases II and III, so they are looking for a driven, growth-oriented Clinical Research Associate to facilitate their in house studies. The CRA will be responsible for: Managing and investigating clinical trials and/or post-authorization safety studies Performing and coordinating different aspects of clinical monitoring and site management 20-25% travel (1x a month) An ideal candidate for this role MUST have… 2+ years of ONSITE monitoring experience at a sponsor or CRO (academia do

*** MUST BE LOCAL TO CA OR NY STATE - NO EXCEPTIONS *** Salary: $100K-$130K Company Summary: A global, specialty pharmaceutical group with an impressive track record is seeking a motivated Clinical Research Associate for a hybrid role at their San Francisco site. Their commercial supply of pharmaceutical products generated $83m in revenue in FY2023 (a 24% uptick from the year prior). Since their first clinical trials in 2006, they've had 3 approvals already on the market. Currently, they have 6 indications in Phases II and III, so they are looking for a driven, growth-oriented Clinical Research Associate to facilitate their in house studies. The CRA will be responsible for: Managing and investigating clinical trials and/or post-authorization safety studies Performing and coordinating different aspects of clinical monitoring and site management 20-25% travel (1x a month) An ideal candidate for this role MUST have… 2+ years of ONSITE monitoring experience at a sponsor or CRO (academia do

*** MUST BE LOCAL TO CA OR NY STATE - NO EXCEPTIONS *** Salary: $100K-$130K Company Summary: A global, specialty pharmaceutical group with an impressive track record is seeking a motivated Clinical Research Associate for a hybrid role at their San Francisco site. Their commercial supply of pharmaceutical products generated $83m in revenue in FY2023 (a 24% uptick from the year prior). Since their first clinical trials in 2006, they've had 3 approvals already on the market. Currently, they have 6 indications in Phases II and III, so they are looking for a driven, growth-oriented Clinical Research Associate to facilitate their in house studies. The CRA will be responsible for: Managing and investigating clinical trials and/or post-authorization safety studies Performing and coordinating different aspects of clinical monitoring and site management 20-25% travel (1x a month) An ideal candidate for this role MUST have… 2+ years of ONSITE monitoring experience at a sponsor or CRO (academia do

Sr. Clinical Research Associate 12-month contract Onsite in Sunnyvale, CA Responsibilities Support the successful execution of clinical studies by contributing to study design, documentation, and overall management. Lead and manage site start-up and activation processes, including regulatory document preparation, IRB/EC submissions, and clinical trial agreements. Conduct monitoring visits (qualification, initiation, interim, and close-out) and ensure protocol and regulatory compliance through source data verification and study oversight. Serve as the primary liaison for clinical sites, overseeing data entry, investigational device tracking, and issue resolution. Maintain and manage study documentation, including Trial Master File (TMF), clinical trial management systems (CTMS), and site payments. Qualifications Experience implementing and managing medical device clinical trials. In-depth knowledge of ISO 14155, 21 CFR Part 11, 50, 54, 812, and ICH/GCP regulations. Proficiency in develo

The in vivo Antibody Discovery group is a specialized team within the Protein Therapeutics function that is responsible for the discovery and optimization of biological drug candidates. We are seeking a highly motivated contingent worker to join this team, with grade level corresponding to Research Associate to Associate Scientist. This is a limited term (6-month) position, with possibility being extended or converted into full time permanent employee. The successful candidate will contribute to antibody discovery efforts as part of a cross-functional team specializing in the discovery and screening of novel biologic modalities in support of all therapeutic areas at the Company. Job Responsibilities: In this laboratory-based role, the successful candidate will support efforts to generate novel antibody-based therapeutics. Ideally, the applicant has a strong foundation in molecular biology, PCR, in vitro mRNA production, and molecular cloning. Job requirements: • Drive antibody discover

Title: Sr. Clinical Research Associate- Contract Location: Remote-based, local to San Francisco. or West Coast required Duration: 6 months Compensation: $85 to $90 depending on experience Please note, this position requires recent (within the last 2-4 years) experience working on the sponsor side of clinical studies. The Senior Clinical Research Associate (Sr CRA) will independently manage all clinical aspects of a small to medium-sized clinical study or, with supervision, assume significant management responsibilities on a large-scale study. This position works closely with a cross-functional team, vendors, sites, and CRO to ensure compliance with protocol and the overall clinical trial objectives. Day to day duties Serves as a crucial member of the project team for the quality execution of assigned clinical protocols according to SOPs, ICH/GCP, and corporate and departmental program goals. Supports the Study Lead as an integral member of a multifunctional team to ensure clinical stud

Title: Sr. Clinical Research Associate- Contract Location: Remote-based, local to San Francisco. or West Coast required Duration: 6 months Compensation: $85 to $90 depending on experience Please note, this position requires recent (within the last 2-4 years) experience working on the sponsor side of clinical studies. The Senior Clinical Research Associate (Sr CRA) will independently manage all clinical aspects of a small to medium-sized clinical study or, with supervision, assume significant management responsibilities on a large-scale study. This position works closely with a cross-functional team, vendors, sites, and CRO to ensure compliance with protocol and the overall clinical trial objectives. Day to day duties Serves as a crucial member of the project team for the quality execution of assigned clinical protocols according to SOPs, ICH/GCP, and corporate and departmental program goals. Supports the Study Lead as an integral member of a multifunctional team to ensure clinical stud