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  1. Head of Preclinical Development-Toxicology

    Head of Preclinical Development and Toxicology with a strong toxicology and immunotoxicity background w/ Experience with pharmacokinetics also desired. Direct experience designing and managing animal toxicology studies and other safety studies, and managing external CROs, as well as other IND enabling activities, including generating reports for FDA submission. Primary responsibilities include all aspects of Preclinical Development including the design, development and direction of toxicology, ...

  2. CMC Technical Writer – Contract (New Jersey)

    DESCRIPTION: Contribute to R&D, LCM and Industrial Development and Innovation projects (in-licensing, partnership projects) by planning, writing and delivering agreed submission deliverables for US, EU and rest of world (ROW) registrations for multiple dosage forms.  Author and create dossier content from source documentation as needed for registrations and provide writing support for technical reports.   Recommend table of contents for regulatory submissions.   Develop and contribute to ...

  3. Clinical Data Management Professional

    Opportunities located: NJ, NY, CT, MA, PA, NC, GA Summary Responsible for collecting data from clinical trials created for pharmaceuticals, biologics, or devices. Ensures data collected is accurate, groups data properly, solves operational problems, and prepares statistical reports. Primary responsibilities Work with complex computerized records systems and maintain security and integrity. Collect data from clinical trials. Sort information and then ensure it's screened, grouped, summarized, ...

  4. Clinical Research Associate

    Opportunities located in: NY, NJ, MA, NC, PA   Summary Responsible for creating, implementing, and maintaining clinical trials. Writes protocols, case report forms, and consent forms. Recruits and selects investigators and ensures good clinical practices are followed. Primary responsibilities Design, implement, and monitor clinical trials. Prepare integrated medical reports, periodic reports, New Drug Applications (NDAs) and Biological License Applications (BLAs). Recruit and select new ...

  5. Business Relationship Manager NYC ( also in CA, DC, TX , OH, FL, MA )

     A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented, performance driven people. All of which makes us one of the most rewarding employers in our field. We're committed to peak performance, improving the quality of life, and embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive advantage.  The Business Relations Manager (BRM) is the key ...

  6. Hematology Supervisor

    Allied Search Partners, the leader in laboratory staffing, is currently working with a client near Levittown, NY to find a qualified and experienced Hematology Supervisor for night shift. Our client is a CAP accredited, leading laboratory offering an extensive testing menu combined with convenience and personalization of service. Know someone for this position? We offer a $$ bonus if we place your referral in a position. Position: Laboratory Supervisor (Hematology) Schedule: 3rd shift/Full ...

  7. Molecular Diagnostics Sales NYC and LI

    Molecular Diagnostics Sales NYC Top Laboratory Diagnostics Company is seeking a sales representative to represent their line of molecular products in the NYC and LI.  Outstanding opportunity for long term career growth. Will sell to all molecular laboratories, including those that are hospital-based.  Exceptional financial package and company benefits. Job Description: Work independently to consistently achieve and exceed (monthly, quarterly, yearly) sales goals as listed in the yearly sales plan ...

  8. FISH/Cytogenetic Technologist

    Per Diem- -Westchester County NY - 3 FISH/Cytogenetic techs (job description below) NYS license a must. Job Title: FISH Cytogenetics Technologist Location: US-NY-Westchester County Overview: Process all specimens for FISH/Cytogenetic testing from accessioning through interpretation. Prepare reagents, buffers and probes according to FDA guidelines. Work up diagnostic medical report including image documentation. Complete QA and QC documentation on a daily basis. Responsibilities: Ability to ...

  9. MANAGER/SR. MANAGER CMC PROJECT MANAGEMENT

    CMC-Manager, or Sr. Manager (Title based on skills and experience). Using extensive CMC Project Management knowledge and experience in the drug development industry, the Manager or Senior Manager leads assigned CMC Projects that are typically of advanced complexity and large scope (such as Commercial or Late Clinical Phase in nature). The Manager/Senior Manager is expected to apply strong supervisory experience to lead and provide CMC expertise/guidance to assigned team members. Essential Duties ...