Jack Altmeyer Email & Phone Number

Boston, Massachusetts, United States

- Consulted on projects across all stages of asset development (preclinical to marketed), involving different types of treatments, including standards of care, gene therapies, and biosimilars- Worked on projects across different indications, including acute myeloid leukemia, myelodysplastic syndrome, cervical cancer, asthma, atopic dermatitis, inflammatory bowel disease, ulcerative colitis, and Duchenne muscular dystrophy- Built competitor landscapes, performed treatment paradigm analyses, crafted competitive threat assessments, and generated implications for client considerations- Synthesized industry themes from market trends, pivotal data readouts, and health care providers’ perceptions- Generated several different types of deliverables, including alerts, monthly and quarterly presentations, approval timeline assumptions, data comparisons, playbooks, as well as pre, peri and post conference outputs based on research and internal recommendations- Monitored news flow, investor relation events, press releases, medical journals and trial databases for clinical, regulatory or commercial updates; collaborated with project team members to analyze findings and develop conclusions- Identified gaps in patient journeys; provided clients with potential clinical impact opportunities and developed tactics to address them - Lead client meetings, researched ad-hoc client requests, and communicated with clients daily- Delegated tasks across projects, reviewed analyst outputs, and provided detailed feedback as needed- Lead project specific trainings for both clients and project teammates- Created guidance documents and templates for project deliverables- Attended conferences to gather perspectives from key opinion leaders

Boston, Massachusetts, United States

- Consulted on projects across all stages of asset development (preclinical to marketed), involving different types of treatments, including standards of care, gene therapies, and biosimilars- Worked on projects across different indications, including acute myeloid leukemia, myelodysplastic syndrome, cervical cancer, asthma, atopic dermatitis, inflammatory bowel disease, ulcerative colitis, and Duchenne muscular dystrophy- Built competitor landscapes, performed treatment paradigm analyses, crafted competitive threat assessments, and generated implications for client considerations- Synthesized industry themes from market trends, pivotal data readouts, and health care providers’ perceptions- Generated several different types of deliverables, including alerts, monthly and quarterly presentations, approval timeline assumptions, data comparisons, playbooks, as well as pre, peri and post conference outputs based on research and internal recommendations- Monitored news flow, investor relation events, press releases, medical journals and trial databases for clinical, regulatory or commercial updates; collaborated with project team members to analyze findings and develop conclusions- Identified gaps in patient journeys; provided clients with potential clinical impact opportunities and developed tactics to address them - Lead client meetings, researched ad-hoc client requests, and communicated with clients daily- Delegated tasks across projects, reviewed analyst outputs, and provided detailed feedback as needed- Lead project specific trainings for both clients and project teammates- Created guidance documents and templates for project deliverables- Attended conferences to gather perspectives from key opinion leaders

Raleigh-Durham-Chapel Hill Area

- First point of contact for Phase II hepatitis and cardiology studies- Gathered and input data into the Clinical Trials Management System (CTMS)- Tracked patient status and study metrics via the Electronic Data Capture (EDC) and Interactive Response Technology (IRT) systems- Reviewed EDC information and invoices submitted by clinical sites against study budgets; initiated the site payment process- Estimated and projected quarterly payment amounts for each site per study- Assisted the Business Development and Vendor Management teams with obtaining and tracking client contact information- Created, developed, maintained, and disseminated multiple study trackers, including trackers concerning regulatory documents, Informed Consent Forms (ICFs), patient status, study contacts, and access to vendor systems- Obtained, processed, reconciled, archived, and tracked all documents for every site per assigned study; reviewed each document for Good Documentation Practice (GDP)- Set-up and maintained the Electronic Trial Master File (eTMF) for all assigned studies- Assisted with internal Quality Assurance reviews and general FDA readiness- Performed internal audits on various eTMFs and located missing documentation- Submitted all necessary study and site information to the Institutional Review Board (IRB) for review and approval- Assisted the Clinical Project Manager and the Lead Clinical Research Associate with managing Sponsor meetings- Created and developed team meeting agendas and minutes- Ordered and distributed supplies to clinical sites - Interfaced directly with Sponsors and distributed study related information to the project team

Raleigh-Durham, North Carolina Area

- First point of contact for multiple oncology studies in various clinical phases- Monitored patient enrollment and dosing, as well as reactions to investigational products, ensuring study sites followed Good Clinical Practice (GCP)- Presented tri-weekly study updates to the entire clinical team - Assisted with Site Start Up and Study Close-Out procedures - Reviewed and queried monitoring reports - Aided the Quality Assurance team with site audits, and developed corrective actions to audit findings- Updated Lab Manuals, Procedure Manuals, and Informed Consent Forms (ICFs) to coincide with current protocols and decisions made by the study team- Prepared Site Initiation, Protocol Amendment, Pharmacy Update, and Tumor/Blood Sample Collection presentations; assisted with study site training- Attended Safety Review Committee meetings and generated meeting minutes for Medical Monitor approval- Assembled, shipped, and tracked clinical lab kits/supplies- Approved weekly investigational product shipments/transfers- Obtained, processed, reconciled, archived, and tracked all documents for every site per assigned study; reviewed each document for Good Documentation Practice (GDP)- Assisted in developing and uploading documents to the first companywide Electronic Trial Master File (eTMF) system- Performed internal audits on various Trial Master Files and located missing documentation- Distributed safety information/updates to study sites, and submitted the necessary information to the Institutional Review Board (IRB) for review and approval- Reviewed and approved accurate invoices from study sites

Winston-Salem, North Carolina

- Investigated the connection between potential RNA methylation and meiosis in fission yeast by utilizing dilution assays, microscope imaging, and reverse transcriptase polymerase chain reaction (RT-PCR) techniques- Determined the growth rates of several mutant fission yeast strains- Analyzed data, generated figures and presented findings of semester long projects to the entire lab team

Camp Hill, Pennsylvania

- Assisted in surgeries including wisdom teeth extractions, dental implants, and jaw reconstructions- Learned the importance of both pre and post-operation patient care; updated families on their patient’s status post-surgery- Washed and sanitized surgical instruments, assembled trays for surgeries, set up and cleaned operation rooms

Hershey, Pennsylvania

- Used Midiprep techniques to prepare DNA for experimental usage- Created figures and diagrams for research presentations- Logged bibliographic information used in research papers- Refilled liquid nitrogen tanks, autoclaved glassware, cleaned fridges and incubators, ordered lab supplies

Bachelor Of Science - Bs, Biology, General

Activities and Societies: New Student Adviser, Alpha Sigma Phi Fraternity, PREPARE Facilitator, Tri-Beta Biological Honor Society

Marine Ecosystems: Monitoring And Management

Jack studied marine biology and conservation, as well as small island tourism on South Caicos, an island in the southern Atlantic, during.