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Clear Point Consultants
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  • Professional Photographer  

    - Westchester County
    NO C2CWe are seeking a detail-oriented Part-Time Photographer to captu... Read More
    NO C2CWe are seeking a detail-oriented Part-Time Photographer to capture clean, accurate product photography that supports internal teams and consumer-facing materials. This is not an artistic or portfolio-building role — it’s a technical photography position focused on consistency, clarity, and precision.Key Responsibilities:Produce silhouetted product images and detailed close-ups of consumer items such as tools, grills, washing machines, and other appliances.Follow established photography scripts and guidelines to ensure every image clearly demonstrates how a product is built or functions.Apply strong lighting skills to create well-exposed, accurate, and consistent images — without stylized or artistic effects.Perform low-level styling (clean and straight setups) to ensure products are presented neatly and clearly, without elaborate composition.Collaborate with editors, writers, and testing teams to ensure visuals align with instructional and documentation needs.Edit, label, and archive photos according to internal asset management standards.Qualifications:2+ years of experience in studio, product, or technical photography.Proficiency with lighting equipment and studio setups.Skilled in Adobe Photoshop and Lightroom for basic editing and retouching.Strong attention to detail and ability to reproduce consistent results.Comfortable following strict visual standards and repeatable workflows.Excellent organizational and communication skills.Preferred Qualifications:Experience photographing mechanical or consumer products.Familiarity with structured, documentation-style photography.Additional Details:Equipment and setup will be provided.Part-time, approximately 20 hours per week.Flexible schedule; occasional onsite work may be required.Compensation commensurate with experience.

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  • Implementation Specialist  

    - Brazos County
    Implementation Specialist opportunity based in College Station, TX (Hy... Read More
    Implementation Specialist opportunity based in College Station, TX (Hybrid – 3 days onsite, 2 remote). This is a full-time, permanent role working onsite, focused on coordinating new customer onboarding and account changes in close partnership with Operations, Supply Chain, and Account Management.The role offers:Base salary of $52,000 plus a 5% bonus (up to $25/hr. equivalent)Full-time, permanent employment with growth potentialA chance to make a direct impact on the customer experience during the most critical phase—getting new sites live accurately and on timeWe’re looking for someone detail-oriented, proactive, and highly organized—comfortable working across teams and keeping customers informed while ensuring deliverables stay on track. Read Less
  • Sales And Marketing Specialist (Boston)  

    - Suffolk County
    We are seeking a highly motivated and results-driven Sales & Marketing... Read More
    We are seeking a highly motivated and results-driven Sales & Marketing Specialist to accelerate growth and expand our client base. This role is responsible for identifying new business opportunities, cultivating strong client relationships, and executing effective marketing strategies to promote our in vivo and in vitro preclinical services. The ideal candidate will have a deep understanding of the preclinical drug development process and a proven track record in sales or business development within the life sciences industry.Key Responsibilities:Sales:Identify, qualify, and pursue new leads through market research, networking, and industry events.Develop and execute strategic sales plans to meet revenue targets.Build and maintain relationships with decision-makers in pharmaceutical, biotech, and academic organizations.Prepare and deliver presentations, proposals, and contract negotiations to close deals.Represent the company at conferences, trade shows, and networking events.Maintain accurate records of sales activities and client interactions in CRM systems.Provide weekly updates to senior management and participate in internal research meetings.Marketing:Develop and implement marketing strategies to enhance brand visibility and generate leads.Create and manage marketing materials, including brochures, website content, and social media posts.Plan and execute campaigns, including email marketing and digital advertising.Analyze marketing metrics and optimize campaigns for performance.Collaborate with scientific staff to generate posters, presentations, and other scientific content.Maintain and update company website content.Market Analysis & Competitive Intelligence:Conduct market research to identify trends, opportunities, and competitive landscape.Monitor competitor activities and provide insights to inform business strategies.Stay current on industry developments and regulatory changes.Qualifications:Bachelors degree in life sciences, business, or related field (advanced degree preferred).Minimum 2 years of experience in sales, business development, or marketing within a preclinical CRO, pharmaceutical, or biotech environment.Strong understanding of the preclinical drug development process, including in vivo and in vitro studies.Proven track record of achieving sales targets and building strong client relationships.Excellent communication, presentation, and negotiation skills.Ability to work independently and collaboratively in a team environment.Proficiency with CRM systems and marketing automation tools.Strong analytical and problem-solving skills.Willingness to travel for conferences and client meetings as needed.Preferred Qualifications:Established network of contacts in pharmaceutical and biotech industries.Experience with specialized in vivo services or specific therapeutic areas.Familiarity with digital marketing strategies and tools.#JO791

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  • As the Senior Manager of Biomarker Operational Quality, youll be the g... Read More
    As the Senior Manager of Biomarker Operational Quality, youll be the go-to person for making sure biomarker-related work across research, clinical trials, and potential commercial use stays aligned with regulatory standards (GxP). Youll work closely with internal teamsespecially Biomarker Ops and GCP Qualityto help drive operational excellence, keep things compliant, and spot potential risks before they become issues.Your job is to help ensure the processes around biomarker developmentincluding those supporting Companion Diagnostics (CDx)are efficient, compliant, and future-ready. Youll also help define and track quality metrics that give a clear picture of how well things are working and where improvements can be made. Youll report to the Director of GCP Biomarker Quality and team up with others in Quality to keep processes consistent across programs and products.What You'll Be Responsible ForPartnering with clinical and preclinical teams to support biomarker quality throughout developmentHelping review regulatory documents (like INDs, IDEs, and trial master files) and calling out potential gapsProviding input for audits focused on GCLP and GCP biomarker-related vendors and activitiesSupporting process and compliance improvements across non-clinical areasJoining cross-functional initiatives to strengthen how the organization meets regulatory standardsFlagging potential compliance issues and helping design smart, realistic solutionsReporting on major quality concerns tied to preclinical developmentLeading or supporting inspection readiness activities for biomarker-related workAdvising on audit strategies for vendors and internal processesHelping assess vendor performance and quality riskAttending key governance meetings and contributing to agendas and metricsCollaborating with stakeholders to define and refine quality indicators for biomarker effortsSharing quality trends and insights with the right people at the right timeProviding quality and compliance oversight for CDx development and validation activities, including alignment with regulatory requirements for diagnostic-device submissions and commercializationPartnering with internal and external stakeholders to ensure CDx-related processes are inspection-ready and meet FDA, EU IVDR, and other global expectationsPossibly contributing to due diligence and integration projectsWhat Youll BringSolid knowledge of lab regulations like CLIA, ISO15189:2022, CLSI, and othersFamiliarity with CDx lifecycle and regulatory pathways for diagnostic productsExperience navigating fast-paced environments and working across teamsFamiliarity with quality metrics, dashboards, and continuous improvementStrong communication skillsyou know how to make quality make senseProblem-solving skills to help resolve issues thoughtfully and quickly

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  • As the Senior Manager of Biomarker Operational Quality, you’ll be the... Read More
    As the Senior Manager of Biomarker Operational Quality, you’ll be the go-to person for making sure biomarker-related work across research, clinical trials, and potential commercial use stays aligned with regulatory standards (GxP). You’ll work closely with internal teams—especially Biomarker Ops and GCP Quality—to help drive operational excellence, keep things compliant, and spot potential risks before they become issues.Your job is to help ensure the processes around biomarker development—including those supporting Companion Diagnostics (CDx)—are efficient, compliant, and future-ready. You’ll also help define and track quality metrics that give a clear picture of how well things are working and where improvements can be made. You’ll report to the Director of GCP Biomarker Quality and team up with others in Quality to keep processes consistent across programs and products.What You'll Be Responsible ForPartnering with clinical and preclinical teams to support biomarker quality throughout developmentHelping review regulatory documents (like INDs, IDEs, and trial master files) and calling out potential gapsProviding input for audits focused on GCLP and GCP biomarker-related vendors and activitiesSupporting process and compliance improvements across non-clinical areasJoining cross-functional initiatives to strengthen how the organization meets regulatory standardsFlagging potential compliance issues and helping design smart, realistic solutionsReporting on major quality concerns tied to preclinical developmentLeading or supporting inspection readiness activities for biomarker-related workAdvising on audit strategies for vendors and internal processesHelping assess vendor performance and quality riskAttending key governance meetings and contributing to agendas and metricsCollaborating with stakeholders to define and refine quality indicators for biomarker effortsSharing quality trends and insights with the right people at the right timeProviding quality and compliance oversight for CDx development and validation activities, including alignment with regulatory requirements for diagnostic-device submissions and commercializationPartnering with internal and external stakeholders to ensure CDx-related processes are inspection-ready and meet FDA, EU IVDR, and other global expectationsPossibly contributing to due diligence and integration projectsWhat You’ll BringSolid knowledge of lab regulations like CLIA, ISO15189:2022, CLSI, and othersFamiliarity with CDx lifecycle and regulatory pathways for diagnostic productsExperience navigating fast-paced environments and working across teamsFamiliarity with quality metrics, dashboards, and continuous improvementStrong communication skills—you know how to make quality make senseProblem-solving skills to help resolve issues thoughtfully and quickly

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  • Sales And Marketing Specialist  

    - Suffolk County
    We are seeking a highly motivated and results-driven Sales & Marketing... Read More
    We are seeking a highly motivated and results-driven Sales & Marketing Specialist to accelerate growth and expand our client base. This role is responsible for identifying new business opportunities, cultivating strong client relationships, and executing effective marketing strategies to promote our in vivo and in vitro preclinical services. The ideal candidate will have a deep understanding of the preclinical drug development process and a proven track record in sales or business development within the life sciences industry.Key Responsibilities:Sales:Identify, qualify, and pursue new leads through market research, networking, and industry events.Develop and execute strategic sales plans to meet revenue targets.Build and maintain relationships with decision-makers in pharmaceutical, biotech, and academic organizations.Prepare and deliver presentations, proposals, and contract negotiations to close deals.Represent the company at conferences, trade shows, and networking events.Maintain accurate records of sales activities and client interactions in CRM systems.Provide weekly updates to senior management and participate in internal research meetings.Marketing:Develop and implement marketing strategies to enhance brand visibility and generate leads.Create and manage marketing materials, including brochures, website content, and social media posts.Plan and execute campaigns, including email marketing and digital advertising.Analyze marketing metrics and optimize campaigns for performance.Collaborate with scientific staff to generate posters, presentations, and other scientific content.Maintain and update company website content.Market Analysis & Competitive Intelligence:Conduct market research to identify trends, opportunities, and competitive landscape.Monitor competitor activities and provide insights to inform business strategies.Stay current on industry developments and regulatory changes.Qualifications:Bachelor’s degree in life sciences, business, or related field (advanced degree preferred).Minimum 2 years of experience in sales, business development, or marketing within a preclinical CRO, pharmaceutical, or biotech environment.Strong understanding of the preclinical drug development process, including in vivo and in vitro studies.Proven track record of achieving sales targets and building strong client relationships.Excellent communication, presentation, and negotiation skills.Ability to work independently and collaboratively in a team environment.Proficiency with CRM systems and marketing automation tools.Strong analytical and problem-solving skills.Willingness to travel for conferences and client meetings as needed.Preferred Qualifications:Established network of contacts in pharmaceutical and biotech industries.Experience with specialized in vivo services or specific therapeutic areas.Familiarity with digital marketing strategies and tools.#JO791

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  • Sales And Marketing Specialist  

    - Suffolk County
    We are seeking a highly motivated and results-driven Sales & Marketing... Read More
    We are seeking a highly motivated and results-driven Sales & Marketing Specialist to accelerate growth and expand our client base. This role is responsible for identifying new business opportunities, cultivating strong client relationships, and executing effective marketing strategies to promote our in vivo and in vitro preclinical services. The ideal candidate will have a deep understanding of the preclinical drug development process and a proven track record in sales or business development within the life sciences industry.Key Responsibilities:Sales:Identify, qualify, and pursue new leads through market research, networking, and industry events.Develop and execute strategic sales plans to meet revenue targets.Build and maintain relationships with decision-makers in pharmaceutical, biotech, and academic organizations.Prepare and deliver presentations, proposals, and contract negotiations to close deals.Represent the company at conferences, trade shows, and networking events.Maintain accurate records of sales activities and client interactions in CRM systems.Provide weekly updates to senior management and participate in internal research meetings.Marketing:Develop and implement marketing strategies to enhance brand visibility and generate leads.Create and manage marketing materials, including brochures, website content, and social media posts.Plan and execute campaigns, including email marketing and digital advertising.Analyze marketing metrics and optimize campaigns for performance.Collaborate with scientific staff to generate posters, presentations, and other scientific content.Maintain and update company website content.Market Analysis & Competitive Intelligence:Conduct market research to identify trends, opportunities, and competitive landscape.Monitor competitor activities and provide insights to inform business strategies.Stay current on industry developments and regulatory changes.Qualifications:Bachelor’s degree in life sciences, business, or related field (advanced degree preferred).Minimum 2 years of experience in sales, business development, or marketing within a preclinical CRO, pharmaceutical, or biotech environment.Strong understanding of the preclinical drug development process, including in vivo and in vitro studies.Proven track record of achieving sales targets and building strong client relationships.Excellent communication, presentation, and negotiation skills.Ability to work independently and collaboratively in a team environment.Proficiency with CRM systems and marketing automation tools.Strong analytical and problem-solving skills.Willingness to travel for conferences and client meetings as needed.Preferred Qualifications:Established network of contacts in pharmaceutical and biotech industries.Experience with specialized in vivo services or specific therapeutic areas.Familiarity with digital marketing strategies and tools.#JO791

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Astrid-Lindgren-Weg 12 38229 Salzgitter Germany