• Support project teams in developing data analyses, methodologies, and client deliverables • Analyze quantitative and qualitative data to generate insights that inform business decisions • Build and maintain data models, dashboards, and reports using Excel and data visualization tools • Translate analytical findings into clear, structured presentations and written summaries • Collaborate with team members to execute project workstreams and meet timelines • Apply structured problem-solving approaches to address client questions and project objectives • Assist in preparing materials for client presentations and internal discussions • Utilize data visualization and reporting tools to enhance analysis and communication • Contribute to continuous improvement of team processes, tools, and workflows • Stay current on life sciences trends and incorporate relevant insights into project work.

Role Description This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Senior Network Consultant - REMOTE. In this role, you will have the unique opportunity to guide our clients through intricate network strategies and solutions, ensuring they are well-equipped to meet current and future challenges. You will work collaboratively with a diverse and talented team dedicated to innovation and excellence. Your influence will extend across organizational levels as you assess, strategize, and drive transformative solutions. With a focus on AI-enabled operations and software-defined networking, you will be at the forefront of technological advancements. Join us and be a part of shaping the future of network architecture and strategy. Accountabilities - Own delivery of network advisory engagements, including scope definition, execution planning, stakeholder coordination, and risk management. - Lead and execute network assessments spanning architecture, design, and operations, with a focus on supporting AI-enabled workloads and AI-driven operations. - Develop and present defensible network strategies and roadmaps that articulate sequencing, tradeoffs, risks, and investment implications for executive stakeholders. - Translate assessment findings into actionable engagement plans that balance operational constraints, technical feasibility, financial considerations, and contractual realities. - Build credibility and influence with stakeholders across technical, operational, and executive levels of client organizations. - Serve as a subject matter expert on the network and operational implications of emerging technologies. - Analyze financial models, proposals, contracts, and statements of work to support sourcing decisions and executive recommendations. - Actively participate in account planning, sales, and solution development within current engagements or prospective clients. Requirements - Travel is less than 25%. - This is a remote position based in the US. - 10 years of relevant work experience, with at least five years in the telecommunications/IT industry. - Ability to work at both the strategic/executive level and the tactical/analyst level. - Demonstrated leadership skills with willingness to take ownership of scope expansion. - Strong consulting, financial modeling, project management, and communication skills. - Working knowledge in network, security, hardware, and software details. - Excellent interpersonal and team-building skills with ability to develop relationships. - Superior verbal communication skills and presentation capabilities. - Self-starter with ambitious over-achiever mindset. - Excellent organizational skills and attention to detail. Benefits - Opportunity for remote work with a flexible schedule. - Collaborative and supportive team environment. - Access to cutting-edge tools and technologies. - Professional development and growth opportunities. - Diversity and inclusion in the workplace. - Competitive salary and performance-based bonuses.

• The New Patient Consultant plays a vital role to the success of CCRM Fertility’s network. • As the first point of contact for the majority of the Network’s potential new patients, this position is critical in setting the tone for the new patient experience. • The New Patient Consultant is responsible for assisting new patients in initiating their CCRM Fertility journey, understanding their options, and ensuring a seamless transition into care. • This role will serve as a liaison between patients and healthcare providers, providing information on the physicians and the CCRM patient experience, and registering patients into the electronic medical record system. • The New Patient Consultant will report to the Practice Administrator. • Adhere to HIPAA regulations and maintain patient confidentiality at all times. • Answer incoming calls with the ultimate goal of aiding the patient in scheduling a new patient appointment. • Communicate information regarding CCRM’s physicians, services, and successes to the potential patient. • Obtain necessary information from the patient including referral source, reason for appointment, demographic information for both patient, spouse, or partner, and insurance information for both. • Work in EMR-system to ensure all patient data is promptly inputted and remains up-to-date. • Send consent forms via DocuSign to both patient, spouse, or partner. • Contact potential patients who have submitted their contact information via CCRM’s website. • Communicate with physicians, clinical/front office staff, and other departments as needed to address patient questions, concerns, and other circumstances. • Maintain and track internal forms and spreadsheets as directed by supervisor. • Attend all staff meetings and in-service meetings. • Other duties as assigned.

Job DescriptionJob TitleConsultant, Process ManufacturingPosition TypeContractorLocationRemoteTravel RequiredTravel may be requiredExternal Posting URLApplications Accepted ByJason C. Bork jason.bork@pintailsolutions.net or (317) 694-0232 (mobile)Mail: Jason C. Bork Pintail Solutions, Suite 104 12172 Visionary Way Fishers, IN 46038Job DescriptionOverview Pintail Solutions is a trusted life science partner improving global health. We work with a variety of clients including CDMO's, biotechs and pharmaceutical companies, CROs, academic institutions, and philanthropic organizations. Clients work with Pintail because of our breadth of experience, our ability to deliver outcomes, and our passion for every project we work on. We focus on the greater good of the client and are fearless about informing clients about what they need instead of what they may ask for. We expect everyone in the company to act like an owner and be insatiable about looking for ways to improve. We value excellence, integrity, and collaboration, and we believe we will make a greater difference in our work when we are having fun doing it. A company is building a commercial-scale peptide Active Pharmaceutical Ingredient (API) manufacturing facility and is seeking a Senior Peptide Manufacturing Consultant to guide process scale-up, facility design, validation, and regulatory readiness for cGMP production. We are seeking an experienced process manufacturing consultant, preferably with peptide manufacturing and continuous flow experience. This engagement is expected to last 9-18 months or longer. This individual will need an entrepreneurial spirit, deep clinical trial experience, preferably from a pharma/sponsor perspective, and a mature business presence to successfully engage with internal and external business partners. Experience is oligos and brain shuttle technology is preferred. The following roles and responsibilities entail most of what this role may be asked to do, but will expand based on the individual’s and organization’s needs. Roles and Responsibilities - Commercial Process Scale-Up - Translate laboratory/pilot peptide processes to multi-kilogram production batches - Optimize synthesis steps (coupling, deprotection, cleavage, yields) - Develop impurity control and solvent usage strategies - Produce a commercial scale-up strategy report - Equipment & Production Capacity Planning - Determine appropriate sizing and throughput for: - Peptide synthesizers - Cleavage reactors - Preparative HPLC systems - Lyophilization equipment - Solvent storage/recovery and waste systems - Build a production capacity model capable of >100 kg/yr output - Facility Design & cGMP Compliance - Review facility layout and workflows - Ensure proper segregation for solvent, resin, cleavage, chromatography, and lyophilization areas - Assess safety and contamination risks - Provide facility design recommendations including utilities - Process Validation & Regulatory Readiness - Help develop: - Process Validation Master Plan (PVMP) - Process Performance Qualification (PPQ) strategy - Cleaning validation for solvent-heavy processes - Continued Process Verification (CPV) - Support preparation for FDA and international inspections - Technology Transfer & Commercial Launch - Create technology transfer packages - Conduct risk assessments (FMEA) - Review batch records - Support commissioning activities including: - FAT/SAT - Engineering runs - PPQ campaigns Qualifications and Education Requirements - 10+ years in peptide API manufacturing - Commercial-scale SPPS/LPPS experience - Regulatory inspection support experience - Large-scale preparative chromatography - Hands-on plant operations experience Preferred Skills - Experience designing or commissioning peptide facilities - Complex/long-chain peptide synthesis - Greenfield facility projects Additional Notes Travel will be required to Indianapolis.