What are the responsibilities and job description for the Clinical Data Manager - Contract (Onsite 3days/wk) position at Jasper Therapeutics?
Jasper is a clinical-stage biotechnology company developing briquilimab, a novel antibody targeting c-Kit (CD117) as a therapeutic for chronic mast and stem cell diseases. Jasper is currently conducting clinical studies of briquilimab as a treatment in patients with CSU or with CIndU and is initiating a clinical study in patients with asthma. Briquilimab is also currently in clinical studies as a treatment for patients with LR-MDS and as a conditioning agent for cell therapies for rare diseases. To date, briquilimab has a demonstrated efficacy and safety profile in more than 160 dosed participants and healthy volunteers, with clinical outcomes in CIndU, and as a conditioning agent in severe combined immunodeficiency (SCID), acute myeloid leukemia (AML), myelodysplastic syndromes (MDS), Fanconi anemia (FA), and sickle cell disease (SCD).
Key Responsibilities
Company Values:
Our mission is to make safer and potentially curative therapy possible for more patients in need. We are bringing together a team of high performing biotech professionals, leading academic institutions and a strong syndicate of healthcare-focused investors to achieve our vision
Key Responsibilities
- Oversee the collection, validation and processing of clinical trial data
- Develop and implement data management procedures for clinical trials
- Support and facilitate the review of medical coding for validity and completeness
- Ensure compliance with applicable regulations, protocols and standard operating procedures in India
- Maintain the highest data quality standards throughout the data lifecycle, from data collection to database lock
- Stay updated on industry best practices, technological advancements and regulatory requirements related to clinical data management
- Develop and maintain data management documentation, including study protocols, case report forms and data management plans
- Design case report forms (CRFs) and electronic data capture (EDC) systems for data collection
- Perform data entry and cleaning activities, including discrepancy management and query resolution
- Conduct data validation checks and implement quality control measures to ensure accuracy and completeness
- Develop and execute standard operating procedures (SOPs) for approval, data entry screen design and testing, validation check testing and approval
- Collaborate with study team members and external vendors, CRO to resolve data-related issues and discrepancies
- Generate and review data listings, summaries and reports for clinical study reports
- Serve as a primary or backup resource for issues about data management
- Ensure compliance with guidelines, Good Clinical Practice (GCP), CDISC standards and other relevant regulations
- Contribute to the development and validation of data management software tools.
- Bachelor’s degree in a scientific or healthcare-related field
- 7-10 years of experience in clinical data management or a similar role in the pharmaceutical or clinical research industry
- Strong understanding of clinical trial processes, data management principles and regulatory guidelines
- Proficiency in electronic data capture (EDC) systems and clinical data management software (e.g. RAVE, Medrio, Veeva)
- Familiarity with relevant regulations and guidelines, like GCP and CDISC standards
- Knowledge of industry-standard data analysis and reporting software, such as SAS, SQL and/or Excel tools
- Excellent attention to detail with problem-solving and analytical skills
- Strong organizational and time management abilities
- SAS programming and certification in clinical data management (like CCDM) a plus
- Knowledge of CRF design, MS Project and analytical capabilities a plus
- Knowledge of CDISC standards and data interchange formats (e.g., SDTM, ADaM) a plus
- Familiarity with clinical trial design and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP)
- Understanding of data privacy and protection regulations (e.g., GDPR)
- Effective communication and interpersonal skills to collaborate with other teams
Company Values:
- Respect
- Collaboration
- Integrity
- Responsible
- Excellence
- Acknowledgment
Our mission is to make safer and potentially curative therapy possible for more patients in need. We are bringing together a team of high performing biotech professionals, leading academic institutions and a strong syndicate of healthcare-focused investors to achieve our vision