Erik Honigmann Email & Phone Number

Mexico

México

Mexico

As a Project Manager specializing in electronic Clinical Outcome Assessments (eCOA) at Signant Health, I lead the planning, execution, and completion of clinical research projects, focusing on integrating advanced project management techniques and ensuring strict adherence to regulatory standards. My role emphasizes enhancing project efficiency and compliance through the following key responsibilities:eCOA Implementation: Led the deployment of eCOA solutions across multiple clinical trials, resulting in a 20% increase in data collection accuracy.Project Timeline and Budget Management: Managed project timelines, budgets, and resources, meeting all milestones and reducing cycle times by 15%.Cross-Functional Collaboration: Facilitated collaboration between cross-functional teams to ensure seamless communication and alignment with strategic goals.Regulatory Compliance: Established and enforced regulatory compliance frameworks, achieving a 100% success rate in submissions for clinical trials.Data Collection Optimization: Optimized data collection processes using electronic systems, greatly improving the accuracy of patient-reported outcomes.Stakeholder Engagement: Influenced stakeholders to adopt innovative solutions, enhancing overall project delivery and increasing client satisfaction.

México

In my role as Regulatory Startup Lead at IQVIA, I managed the execution of regulatory startup activities across multiple clinical trials, ensuring that all projects were in full compliance with regulatory requirements. My leadership in this role co-ordinated to the successful initiation and smooth execution of clinical studies, meeting critical deadlines and enhancing the overall efficiency of the regulatory process.Administered RSU processes for over 15 clinical trials, ensuring 100% compliance with global regulatory standards and reducing startup timelines by 20%.Liaised with cross-functional teams, including clinical operations, data management, and external vendors, to coordinate and facilitate the submission of essential regulatory documents.Influenced stakeholders to adopt innovative regulatory strategies, resulting in a streamlined approval process and faster market entry for new therapies.Managed all aspects of regulatory submissions, from the initial planning stages through to final approval, ensuring that all submissions were accurate and on time.Established strong relationships with regulatory authorities, leading to expedited reviews and approvals.Coordinated risk assessments and implemented mitigation strategies to address potential regulatory challenges, maintaining a high level of project integrity.

México

As a Sr Global Clinical Trial Assistant, I played a pivotal role in supporting the global clinical development operations (GCDO) team by managing various aspects of clinical trials, including protocol management, trial budgets, and vendor coordination. My efforts ensured that clinical trials were completed on schedule and adhered to regulatory standards.Coordinated clinical trial protocols, working closely with cross-functional teams to keep all trial activities on track.Led the tracking of study timelines and budgets, achieving a 10% improvement in project delivery time and cost reduction.Implemented a system for managing trial-specific documents and investigator meetings, enhancing document access and improving meeting productivity by 15%.Managed communication between the study team and external vendors, ensuring prompt delivery of services and materials needed for trial execution.Monitored and reported on trial progress, delivering essential updates to senior management and stakeholders, resulting in better decision-making.Drove the successful closure of multiple clinical trials by ensuring comprehensive data collection, documentation, and submission in line with regulatory requirements.

México

In my role as a Study Management Associate, I oversaw the operational aspects of clinical studies, ensuring alignment with study protocols and regulatory requirements. I prepared and coordinated with study teams and external vendors to facilitate the smooth execution of clinical trials.Pioneered the daily operational activities of clinical studies, ensuring that all milestones were met according to timelines and budget.Developed communications between study teams, investigators, and external vendors, ensuring clear and consistent information flow.Facilitated the preparation and submission of regulatory documents, ensuring compliance with industry standards and guidelines.Implemented tracking systems for study progress, leading to a 10% reduction in delays and improved adherence to timelines.Coordinated the training of study site staff on protocol procedures, enhancing protocol compliance and data accuracy.

Ciudad De México Y Alrededores, México

Perform sample processing and molecular diagnostic tests.Maintain diagnostic equipment and control reagents.Provide scientific technical support.Ensure compliance with safety and quality standards.

México

Professional practicesResponsibilities:• Presentation on auto inflammatory diseases• Review and discussion of scientific articles for their participation in a competition• Selection and isolation of clinical samples of research interest, DNA extraction, amplification of DNA, polymerase chain reaction (PCR)

Professional Practices and social service• Responsibilities:• Perform different types of diagnostic molecular tests:• Enzyme-linked immunosorbent assays (ELISA)• Western blot• DNA extraction• Sample treatment (acridine orange) for reading in the fluorescence microscope, reading of lamellae to detect micronuclei in reticulocytes• Implementation of a waste treatment method to make them less toxic for the environment• Exhibition of scientific articles in seminars• Discussion of the results obtained during the week• Propose solutions to the problems presented• Organized information by studying, analyzing, interpreting and classifying data

ScholarshipResponsibilities:• Receive patients• Register patients• Perform electrocardiograms• Conferred with multidisciplinary healthcare team to help effectively manage patient conditions with regular testing and vitals assessments• Cleaned and prepared rooms between patients, using aseptic technique to prevent infections and cross-contamination• Assisted patients with mobility needs, including moving to and from beds, organizing wheelchairs and preparing assistive devices• Documented patient symptoms, medical histories and current medications

Micromaster, Statistics And Data Science

Activities and Societies: Data Analysis, Machine learning algorithmsLearning in the fundamentals of probability and statistics, as well.

Certificate, Agile Project Management

Mastered Scrum mechanics and translated other Agile frameworks such as SAFe, Disciplined, and LeSS. Gained expertise in applying Agile.

Diploma, High Direction/Administration / Management Of Health Centers And Hospitals

• Training in the area on High Direction, Management and Hospital Administration, with a concrete knowledge in the development.

Diploma, Conduction And Monitoring Of Clinical Research Study

This program develops healthcare professionals in clinical trial management through seven focused modules, covering pharmacology, trial.

Certificate, English

Diploma, Advanced Immunology

• Knowledge advanced and deep on this biomedical area

Certification, Immunology, Elisa-Alegria

Activities and Societies: • Coursework in ELISA, ALEGRIA equipmentTraining taken in Frankfurt-Germany

Licentiate Degree, Diagnostic Biochemistry

Activities and Societies: Speaker at Symposium XX Metabolic Diseases. Work with low-frequency magnetic fields in chronic degenerative.