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Meet Life Sciences
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  • Vice President Research And Development  

    - Ventura County
    Meet is working with a startup biotech out of the Thousand Oaks area l... Read More
    Meet is working with a startup biotech out of the Thousand Oaks area looking to hire a VP/SVP of Biology. Their science is groundbreaking and this is an amazing opportunity to join during a very pivotal time. You will lead the end-to-end biology function across all programs driving high quality data generation, operational excellence, and team's performance while shaping biology strategy, cross functional alignment, and securing resources to advance the portfolio. Requirements: PhD in molecular/cellular biology, biochemistry, pharmacology or related discipline. Experience leading biology functions including in vitro, in vivo, to drive programs from exploratory biology through pre-clinical nomination. Proven leadership operating at a strategic and operational level, managing and developing high-performing biology teams (in vitro leads) and delivering rigorous decision enabling data packages that integrate medicinal chemistry, in vivo pharmacology, DMPK, toxicology, and program leadership. Experience with multiple successful INDs, NDAs, and equivalents. Please apply directly if your experience aligns. Read Less
  • Vice President Clinical Development  

    - San Mateo County
    Vice President, Clinical Development Small Biotech | Immuno-Oncology |... Read More
    Vice President, Clinical Development Small Biotech | Immuno-Oncology | Late-Phase Leadership I'm partnering with an innovative, well-backed small biotech seeking a VP, Clinical Development to lead strategy and execution across a late-stage immuno-oncology portfolio. This is a highly visible executive role with the opportunity to shape overall clinical direction, influence corporate strategy, and work closely with the C-suite and Board. Key Responsibilities: • Define and lead global clinical development strategy across late-phase programs • Provide executive oversight of Phase II/III trials, including design, execution, and data interpretation • Drive regulatory strategy and represent the company in health authority interactions • Partner cross-functionally across regulatory, translational sciences, biometrics, commercial, and medical affairs • Serve as a key external ambassador with KOLs, investigators, partners, and investors Ideal Profile: • MD required, board-certification in oncology strongly preferred • Deep immuno-oncology expertise • HCC (hepatocellular carcinoma) experience strongly preferred • Proven late-phase (Ph II/III) leadership experience • Strong track record of regulatory engagement and filings • Strategic thinker who is equally comfortable being hands-on in a lean biotech environment This is a rare opportunity to step into a true leadership seat where you will directly impact pipeline strategy and patient outcomes in a dynamic, entrepreneurial setting. For a confidential discussion, please reach out: tanya.kochan@meetlifesciences.com Read Less
  • Vice President Clinical Development  

    - San Francisco County
    Vice President, Clinical Development Small Biotech | Immuno-Oncology |... Read More
    Vice President, Clinical Development Small Biotech | Immuno-Oncology | Late-Phase Leadership I'm partnering with an innovative, well-backed small biotech seeking a VP, Clinical Development to lead strategy and execution across a late-stage immuno-oncology portfolio. This is a highly visible executive role with the opportunity to shape overall clinical direction, influence corporate strategy, and work closely with the C-suite and Board. Key Responsibilities: • Define and lead global clinical development strategy across late-phase programs • Provide executive oversight of Phase II/III trials, including design, execution, and data interpretation • Drive regulatory strategy and represent the company in health authority interactions • Partner cross-functionally across regulatory, translational sciences, biometrics, commercial, and medical affairs • Serve as a key external ambassador with KOLs, investigators, partners, and investors Ideal Profile: • MD required, board-certification in oncology strongly preferred • Deep immuno-oncology expertise • HCC (hepatocellular carcinoma) experience strongly preferred • Proven late-phase (Ph II/III) leadership experience • Strong track record of regulatory engagement and filings • Strategic thinker who is equally comfortable being hands-on in a lean biotech environment This is a rare opportunity to step into a true leadership seat where you will directly impact pipeline strategy and patient outcomes in a dynamic, entrepreneurial setting. For a confidential discussion, please reach out: tanya.kochan@meetlifesciences.com Read Less
  • Manager, Clinical Contracts  

    - Sonoma County
    Company Our client is an innovative, well-funded biotechnology company... Read More
    Company Our client is an innovative, well-funded biotechnology company focused on advancing cutting-edge research aimed at understanding and treating complex diseases associated with aging. The team operates in a highly collaborative environment that values curiosity, rigor, and impactful science. Role Overview We are seeking an experienced and highly organized Manager, Clinical Contracts (contractor) to support clinical development teams with vendor contracting activities with a specific focus on CMC including clinical supply and manufacturing and biomarker or lab-related contracts This is a 12-month renewable contract. The role is hybrid, requiring three to four days per week onsite in San Francico, providing regular collaboration with internal teams and cross-functional stakeholders. Key Responsibilities Draft, negotiate, and finalize agreements with clinical vendors with emphasis on CMC and biomarker or lab vendors in a timely and efficient manner Partner closely with department leaders to identify evolving vendor scope, budget adjustments, and additional contracting needs related to clinical supply, manufacturing, and lab services Track contract budgets and percentage of completion using internal tools and templates to support financial oversight of vendor agreements Manage a high volume of contracting activities across multiple fast-moving clinical programs with focus on scientific, manufacturing, and laboratory deliverables Support governance initiatives by monitoring and reporting on key performance indicators Work with internal stakeholders and Clinical Operations teams to clarify vendor roles, responsibilities, and operational expectations particularly for CMC and lab or biomarker work Identify and monitor vendor-related issues and coordinate appropriate resolution Assist in vendor sourcing efforts including evaluating vendor capabilities and fit for CMC, biomarker, and laboratory projects Collaborate with cross-functional teams to track deliverables, manage workflow, and maintain clear communication across departments Ideal Candidate Profile 5 plus years of experience in vendor contracting, outsourcing, vendor management, or a related function within life sciences, preferably with experience in CMC or lab and biomarker contracts Strong proficiency in Microsoft Word and Excel with experience tracking budgets and reviewing financial data Excellent communication and interpersonal skills with the ability to work effectively across cross-functional teams Strong organizational skills with the ability to prioritize multiple tasks while maintaining strong internal stakeholder relationships Comfortable working in a fast-paced, evolving environment where priorities may shift A hands-on contributor who takes initiative, follows through, and enjoys execution-focused work Read Less
  • Research Associate | In-Vivo Pharmacology  

    - Ventura County
    About the Company A growing biotechnology organization with a strong p... Read More
    About the Company A growing biotechnology organization with a strong preclinical pipeline is focused on advancing novel therapeutic programs for serious diseases. The company emphasizes high-quality in vivo data generation to support early discovery and translational research. The environment is hands-on, collaborative, and well-suited for scientists who enjoy daily bench and animal work within a close-knit research team. About the Role We are hiring an In Vivo Research Associate to support day-to-day animal studies at an onsite research facility in Thousand Oaks, CA. This is a 40-hour/week contract role with potential for long-term employment This is a hands-on position focused on routine in vivo work rather than advanced or complex surgical techniques. The ideal candidate has prior experience working with laboratory animals and is comfortable performing standard procedures as part of a collaborative in vivo team. Responsibilities Daily care and handling of laboratory animals in compliance with approved protocols Performing routine in vivo procedures such as dosing, blood collection, tissue harvesting, and necropsy Supporting animal colony maintenance and general vivarium-related activities Assisting with in vivo pharmacology studies, including sample collection and basic data recording Maintaining accurate records and study documentation, including use of spreadsheets and electronic systems Preparing work areas and equipment for animal procedures Working closely with in vivo team members and collaborating with scientists across functions Qualifications Prior hands-on experience working with laboratory animals (academia or industry) Approximately 3+ years of experience supporting animal colonies or in vivo studies preferred Comfortable with routine animal handling, dosing, and tissue collection Experience in an academic lab or while completing a degree is acceptable Basic wet-lab skills; exposure to assays such as PCR or Western blotting is a plus but not required Strong organizational skills and comfort working with Excel spreadsheets and routine documentation Reliable, detail-oriented, and collaborative with a strong work ethic Education level and institution are flexible; practical animal experience is the priority Read Less
  • Senior Medical Director  

    - Santa Clara County
    Senior / Executive Medical Director, Clinical Development Small Biotec... Read More
    Senior / Executive Medical Director, Clinical Development Small Biotech | Immuno-Oncology | Late-Phase Focus I'm partnering with a highly innovative small biotech seeking a Senior or Executive Medical Director, Clinical Development to play a key leadership role in advancing their immuno-oncology pipeline. This is a hands-on, strategic position offering significant visibility and impact within a nimble, science-driven organization. Key Responsibilities: • Lead and execute late-phase clinical development strategy • Serve as the clinical lead for immuno-oncology programs • Drive protocol development, study oversight, and data interpretation • Partner cross-functionally with regulatory, translational, and commercial teams • Represent the program externally with KOLs, investigators, and regulators Ideal Profile: • MD required, board certification in oncology strongly preferred • Strong experience in immuno-oncology • HCC (hepatocellular carcinoma) experience strongly preferred • Late-phase (Ph II/III) development leadership • Ability to operate both strategically and tactically in a lean biotech setting • Proven regulatory interaction experience This is an opportunity to shape clinical strategy and directly influence the trajectory of promising oncology programs in an entrepreneurial environment. If you're interested in learning more, or know someone who could be a strong fit, please reach out for a confidential discussion: tanya.kochan@meetlifesciences.com Read Less
  • Manager Medical Writing  

    - San Mateo County
    Key Responsibilities Document Leadership and Authoring: Provides medic... Read More
    Key Responsibilities Document Leadership and Authoring: Provides medical writing leadership for clinical programs Acts as a medical writing subject matter expert and collaborates with the Clinical Science team to deliver on clinical documents including clinical study protocols and protocol-related documents (e.g. informed consent forms), clinical study reports, DSURs, Investigator's Brochures, IND clinical summaries/overviews, and CTD components (e.g. Module 2 summaries) Partners with the regulatory function to ensure timely completion of high-quality regulatory documents including health authority meeting requests, briefing packages, responses to requests for information, and other documents as required for submissions Vendor Management: Provides guidance to external writers on prioritization, content and timeline development, and process management to support clinical development and regulatory activities Process Improvement: Develops medical writing best practices Partners with the Quality Assurance team to develop new and update existing Standard Operating Procedures for Medical Writing processes and all clinical documents to ensure compliance with ICH requirements Position Requirements Master's degree in a life science discipline from an accredited college or university; PharmD or PhD preferred Minimum of 8+ years of scientific or medical writing experience at a biotech/ pharmaceutical company or clinical research organization setting Expert knowledge of standard clinical regulatory document types and associated regulatory requirements (e.g. ICH guidance, FDA, EMA, Health Canada, Asia-Pacific regulations, etc.) Prior writing experience in Clinical Study Protocols, Clinical Study Reports, DSUR, Investigator's Brochures, IND clinical summaries/overviews, CTD clinical summaries, and partnering with external investigators to support Investigator Initiated Study Trials Expert ability of Microsoft Office Suite, Adobe Acrobat, collaborative review management systems (e.g. SharePoint) and documents management (e.g. Veeva RIM) Experience in resource planning and management experience of contractors Excellent organization skills with a passion for delivering quality results Detail-oriented mindset with excellent verbal and written communication skills Self-motivated and able to work collaboratively Ability to roll up sleeves in a start-up environment and a positive can-do attitude Must be willing to work onsite at least 4 days a week Read Less
  • Medical Director  

    Associate Medical Director/Medical Director, Clinical Development - Sa... Read More
    Associate Medical Director/Medical Director, Clinical Development - San Francisco Bay Area (Hybrid) We are partnering with an innovative clinical-stage biotech company with a robust and diverse oncology pipeline to appoint an Associate Medical Director or Medical Director, Clinical Development . This is a high-impact opportunity to join a growing organization at an exciting stage of development, with multiple assets progressing across clinical phases. As a key member of the Clinical Development team, you will contribute to the strategic planning and execution of late-stage oncology clinical programs, working cross-functionally to advance novel therapies toward registration and commercialization. This role is ideal for: A clinically practicing oncologist looking to transition from academia into industry OR A physician with 1–2 years of biotech/pharma industry experience in oncology clinical development ready for broader responsibility Candidates must have hands-on clinical experience treating patients. Key Responsibilities Contribute to clinical development strategy across oncology programs Lead or support protocol design and study oversight (Phase I–III) Provide medical monitoring and scientific leadership Author and review key clinical and regulatory documents Engage with KOLs, investigators, and advisory boards Partner cross-functionally with Clinical Operations, Regulatory, Translational Science, and Commercial Requirements MD (or equivalent) with oncology training (board-certified/eligible preferred) Active clinical practice background with direct patient care experience Strong scientific rigor and understanding of oncology drug development Excellent communication and stakeholder engagement skills Entrepreneurial mindset suited to a biotech environment Able to come onsite 3 days/week in the San Francisco Bay Area Why This Role? Join a biotech with a robust, well-funded pipeline and clear development milestones Meaningful strategic input and visibility with senior leadership Opportunity to shape programs from early development through late-stage trials Competitive compensation package If you are an oncologist motivated to bring innovative therapies to patients and want to be part of a dynamic biotech journey, we would welcome a confidential conversation. Apply via LinkedIn or email me at tanya.kochan@meetlifesciences.com if interested. Read Less
  • Senior Manufacturing Process Engineer  

    - Sonoma County
    Senior Manufacturing Process Engineer Meet has partnered with an excit... Read More
    Senior Manufacturing Process Engineer Meet has partnered with an exciting Stealth start-up in the Brain-Computer Interface (BCI) space based in the San Francisco Bay area. The company is developing cutting-edge medical devices and technology for the treatment of unmet neurological disorders. The Head of Operations is seeking an experienced Manufacturing Process Engineer to support NPI of electro-mechanical devices in collaboration with suppliers. This role will focus on hands-on interaction with suppliers to develop manufacturing processes, tooling, and documentation, from design feasability through commercial release. This role will require real-time engagement and technical support of suppliers, and this individual will be expected to travel often to domestic supplier sites and occasionally to international suppliers. Primary Responsibilities: Serve as the primary technical liaison to external manufacturing partners, ensuring successful delivery of components, assemblies, and finished devices Collaborate with product development teams to ensure designs are manufacturable and compliant with medical device quality system requirements Develop and maintain manufacturing documentation, including work instructions, process flows, and validation protocols Support supplier implementation of specifications, manufacturing processes, and quality requirements Lead and participate in process validation activities including IQ/OQ/PQ, PFMEA, and failure investigations Drive continuous improvement initiatives related to manufacturing efficiency, quality, cost, and scalability Support resolution of non-conformances and corrective actions with suppliers Ensure manufacturing activities comply with applicable regulatory requirements (FDA, ISO 13485, EU MDR, etc.) Provide hands-on technical support to suppliers, including travel as needed (domestic and international) Role Requirements: B.S. in relevant engineering discipline, or equivalent experience. 10 or more years of medical device manufacturing experience, preferably in senior roles at start-up companies developing and manufacturing electro-mechanical devices. Experience with active implantable systems (Implant, Leads, Externals, etc.). Experience with medical device manufacturing including molding, laser welding, clean room assembly, packaging, labeling, and sterilization. Experience with electronic manufacturing and test including PCB fab, PCA assembly, microelectronics assembly, flip chip, in circuit test (ICT) and functional test. Experience with manufacturing automation. Experience in defining and executing process validation activities. Experience collaborating with internal customers and external partners. Understanding of and experience implementing validating manufacturing processes for medical devices in accordance with FDA and EU Requirements. Experience with Solidworks, Labview / manufacturing process and test automation software. Ability to travel to Domestic and International supplier sites frequently Read Less
  • Medical Director  

    - Santa Clara County
    Associate Medical Director/Medical Director, Clinical Development - Sa... Read More
    Associate Medical Director/Medical Director, Clinical Development - San Francisco Bay Area (Hybrid) We are partnering with an innovative clinical-stage biotech company with a robust and diverse oncology pipeline to appoint an Associate Medical Director or Medical Director, Clinical Development . This is a high-impact opportunity to join a growing organization at an exciting stage of development, with multiple assets progressing across clinical phases. As a key member of the Clinical Development team, you will contribute to the strategic planning and execution of late-stage oncology clinical programs, working cross-functionally to advance novel therapies toward registration and commercialization. This role is ideal for: A clinically practicing oncologist looking to transition from academia into industry OR A physician with 1–2 years of biotech/pharma industry experience in oncology clinical development ready for broader responsibility Candidates must have hands-on clinical experience treating patients. Key Responsibilities Contribute to clinical development strategy across oncology programs Lead or support protocol design and study oversight (Phase I–III) Provide medical monitoring and scientific leadership Author and review key clinical and regulatory documents Engage with KOLs, investigators, and advisory boards Partner cross-functionally with Clinical Operations, Regulatory, Translational Science, and Commercial Requirements MD (or equivalent) with oncology training (board-certified/eligible preferred) Active clinical practice background with direct patient care experience Strong scientific rigor and understanding of oncology drug development Excellent communication and stakeholder engagement skills Entrepreneurial mindset suited to a biotech environment Able to come onsite 3 days/week in the San Francisco Bay Area Why This Role? Join a biotech with a robust, well-funded pipeline and clear development milestones Meaningful strategic input and visibility with senior leadership Opportunity to shape programs from early development through late-stage trials Competitive compensation package If you are an oncologist motivated to bring innovative therapies to patients and want to be part of a dynamic biotech journey, we would welcome a confidential conversation. Apply via LinkedIn or email me at tanya.kochan@meetlifesciences.com if interested. Read Less

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