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You searched for Biotech Jobs in New York, NY

Sales: Sales Biotech - Great Neck, New York (LocalJobBoard)
Great Neck, NY -- Job DescriptionWe are seeking 1099 salespeople for a new product that is at the cusp of biotech

IP Transaction Associate - pharma and biotech Job (The Job Spider)
New York, NY -- in the pharma and biotech field. Background in life sciences. Academic excellence Solid law firm background.

Executive: Director of Software Engineering (Biotech, Cloud (LocalJobBoard)
New York, NY -- -on programming and has background in the Healthcare, Life Sciences, Biotech industry. The perfect candidate

IT / Software / Systems: Director of Software Engineering (Biotech, Cloud (LocalJobBoard)
New York, NY -- -on programming and has background in the Healthcare, Life Sciences, Biotech industry. The perfect candidate

IT / Software / Systems: Director of Software Engineering (Biotech, Cloud (LocalJobBoard)
New York, NY -- -on programming and has background in the Healthcare, Life Sciences, Biotech industry. The perfect applicant

Patent Agent/Advisor with 1+ year of biotech experience (BCG Attorney Search)
New York, NY -- New York City office of our client seeks patent agent/advisor with 1+ year of biotech background

Clinical Operations Manager: Innovative Biotech Co., New York quot;No (Advertigo)
New York, NY -- Clinical Operations Manager Innovative Biotech Co. New York North NJ area Summary Our client

Sales: AR / VR Sales (Pharma - Biotech) - New York, New York (LocalJobBoard)
New York, NY -- experience selling SaaS to Pharma Manufacturers or Biotech? Our transformative software has been deployed

Senior Python Developer - BioTech Startup Changing Pharma (Dealslister)
New York, NY -- growing BioTech startup that is revolutionizing the Pharmaceutical Industry? If yes to all 3, read on We

Regulatory Manager (MyBiotechCareer)
Parsippany, NJ -- Our client, a leading pharmaceutical company, is currently seeking an accomplished Regulatory Manager to join the team. Here is an overview of the role: 1) Provide regulatory strategies for products, including regulatory consultations, product description and security assessments for well-received and timely submissions 2) Ensure project plans are in alignment with submission strategies and regulatory guidelines 3) Evaluate and write regulatory credentials for various regulatory agencies 4) Prepare compliance packages for regulatory agencies in fulfillment with applicable necessities and best practice 5) Participate in Multidisciplinary Assignment Team within the Market Access Department 6) Review, manage and track submission and maintenance processes to support regulatory applications 7) Classify meetings within the Market Access Department with the goal of maintaining up-to-date knowledge of existing and proposed regulatory credentials

Director of Clinical Research (MyBiotechCareer)
New York, NY -- Our client, a leading life sciences company, is currently recruiting a Director of Clinical Research who will infuse the Clinical Research Team with their talent, energy and leadership skills. This is an exceptional opportunity to join a corporate culture that is known for its innovative and growth-oriented vision. Assignments include: 1) Direct and implement clinical research plans and programs according to recognized design principles 2) Lead the development of clinical protocol to gather clinical development plan objectives 3) Serve as a Medical Supervisor and Clinical Programmer and review safety data 4) Implement strategies to identify, supervise and resolve clinical program or trial issues 5) Serve as an expert to provide direction to all project team functions 6) Identify and liaise with KOLs concerning program plan and systematic advice 7) Interpret study data and develop integrated review of safety and efficiency 8) Set key deadlines and project milestones for projects within the function

Senior Manager of Clinical Operations (MyBiotechCareer)
New York, NY -- Our client, a leading pharmaceutical company, is currently seeking an accomplished Senior Manager of Clinical Operations to join the team. Here is an overview of the role: 1) Devise strategies and plans for the Clinical Department according to workplace standards 2) Plan and oversee all patient care and clinical operations and programs 3) Recruit employees to ensure department is staffed with qualified personnel 4) Assign cases and create schedules for all employees 5) Coordinate and supervise staff by providing constructive feedback 6) Provide personnel with clinical training and opportunities for continuous development 7) Evaluate performance and discipline employees, when necessary 8) Monitor compliance with legal guidelines, internal policies and quality standards 9) Perform other duties as assigned

Director of Clinical Operations (MyBiotechCareer)
Locust Valley, NY -- A leading company in the pharmaceutical industry is currently seeking a Director of Clinical Operations to join their team. The role will be challenging but also highly rewarding and this leader will be a key voice in the company. For the right executive, this is a fantastic opportunity with great growth prospects. Key duties include: 1) Lead the regulatory strategy and comply with all product development programs 2) Ensure that development programs are well controlled and conducted accurately 3) Develop and implement product regulatory strategy 4) Oversee proper selection of clinical / non-clinical vendors, CROs and independent consultants 5) Ensure success of company goals via adherence to project timelines and budgets 6) Comply with regulatory authorities for new drug application programs 7) Develop, implement and maintain SOPs for all aspects of the department 8) Oversee overall quality and comply with all regulatory submissions 9) Participate with business development team for various tasks

Project Manager (MyBiotechCareer)
New Hyde Park, NY -- Our client, a leading pharmaceutical company, is currently seeking an accomplished Project Manager to join the team. Here is an overview of the role: 1) Lead and manage the setup of multiple clinical trials, including preparation of study specific set up documents and manuals 2) Collect and process samples in close collaboration with the Logistics and Sample Handling departments 3) Monitor projects to ensure they are completed in time, budget and schedule 4) Supervise daily tasks assigned to the Project Assistant per SOPs and project-specific timelines 5) Interact with sponsors and sites for clinical projects to ensure continuity of customer service for other projects as required 6) Manage changes in project scope, schedules and costs 7) Coordinate internal resources and 3rd parties or vendors for the flawless execution of projects 8) Ensure that all projects are delivered on-time, within scope and within budget 9) Establish a detailed project plan to track progress

Senior Director of Clinical Development (MyBiotechCareer)
Manhattan, NY -- A leading company in the pharmaceutical industry is currently seeking a Senior Director of Clinical Development to join their team. The role will be challenging but also highly rewarding and this leader will be a key voice in the company. For the right executive, this is a fantastic opportunity with great growth prospects. Key duties include: 1) Prepare protocols, brochures, report forms and medical reports 2) Execute efficient programs based on the necessary standards 3) Represent the company in front of experts 4) Recruit, screen and select competent sites and investigators 5) Organize investigators’ meetings and conduct other relevant activities to support developed objectives 6) Develop timetable, budget and resource analysis for various programs 7) Design, implement and monitor clinical trials for successful product approvals 8) Review clinical data and write clinical reports upon completion of clinical studies 9) Ensure that Good Clinical Practices are followed

Senior Scientific Medical Liaison (MyBiotechCareer)
South Plainfield, NJ -- Our client, a leading biotechnology company, is currently seeking an accomplished Senior Scientific Medical Liaison to join the team. Here is an overview of the role: 1) Pertain business training, background and scientific sharpness 2) Compel new business opportunities in the precision and personalized medicine sector 3) Build relationships with members of the medical and healthcare business community 4) Impart scientific advice to insurance payers to accomplish reimbursement strategies 5) Maintain novel strategies for on-line marketing of diagnostic health apps 6) Identify and support new opportunities for growth by tracking medical and industry developments 7) Analyze, interpret and write up scientific results for medical publications and conferences 8) Develop logical research skills to efficiently convey the value of products to clinicians 9) Classify and perform new business models for molecular diagnostic products

Quality Compliance Manager (MyBiotechCareer)
Ramsey, NJ -- Our client, a leading pharmaceutical company, is currently seeking an accomplished Quality Compliance Manager to join the team. Here is an overview of the role: 1) Collaborate and support formulation development, technical process operations and analytical services 2) Manage Quality Compliance activities for customers 3) Track, trend and approve CAPA Quality system 4) Monitor and examine product quality complaints 5) Oversee annual product reviews for products 6) Perform and oversee the internal and external audit quality system 7) Assess quality agreements between GAT and clients for completeness and accuracy 8) Coordinate the prompt distribution of documents 9) Conduct trend analysis assessment and prepare a quarterly and annual presentation for management review 10) Investigate and prepare reports for incidents, deviations, failures, complaints and corrective/preventive actions 11) Lead the development of training programs with each department for new and current employees’ techniques

Director of Clinical Research (MyBiotechCareer)
Westwood, NJ -- Our client, a leading life sciences company, is currently recruiting a Director of Clinical Research who will infuse the Clinical Research Team with their talent, energy and leadership skills. This is an exceptional opportunity to join a corporate culture that is known for its innovative and growth-oriented vision. Assignments include: 1) Direct and implement clinical research plans and programs according to recognized design principles 2) Lead the development of clinical protocol to gather clinical development plan objectives 3) Serve as a Medical Supervisor and Clinical Programmer and review safety data 4) Implement strategies to identify, supervise and resolve clinical program or trial issues 5) Serve as an expert to provide direction to all project team functions 6) Identify and liaise with KOLs concerning program plan and systematic advice 7) Interpret study data and develop integrated review of safety and efficiency 8) Set key deadlines and project milestones for projects within the function

Staff Regulatory Affairs Specialist (MyBiotechCareer)
Franklin Lakes, NJ -- We are seeking a driven individual with a passion for the medical device industry. 1 of our clients is looking to add a strong Regulatory Affairs Specialist to their team. Assignments include: 1) Maintain universal registration of products 2) Lead regulatory efforts required to comply with new regulations and qualifications 3) Work carefully with informed bodies and pharmaceutical partners to ensure registrations are up-to-date 4) Create close partnership with pharmaceutical customers and also develop understanding of customer’s regulatory policies 5) Review promotional and advertising materials to ensure regulatory compliance, as assigned 6) Collect suitable data for regulatory submissions and compliance 7) Identify ways to improve efficiency of current work processes 8) Keep the relevant team and supervisors informed about the potential impacts 9) Perform other duties as assigned

Medical Director of Clinical Research and Development (MyBiotechCareer)
New York, NY -- Our client, a leading pharmaceutical company, is currently recruiting a Medical Director of Clinical Research and Development who will infuse the Clinical Research and Development Team with their talent, energy and leadership skills. This is an exceptional opportunity to join a corporate culture that is known for its innovative and growth-oriented vision. Assignments include: 1) Communicate effectively with partners, affiliates and stakeholders 2) Ensure adjustments and time-bound clinical and business commitments 3) Follow GCP and GVP, aligned with technical qualifications for products 4) Meet the unmet needs of iron deficiency 5) Drive quality culture and core competency model initiatives 6) Characterize unmet needs of areas under development 7) Inform about business development opportunities 8) Lead the Professional Team on evidence generation and synthesis 9) Perform other duties as assigned

Director of Product Development (MyBiotechCareer)
Lyndhurst, NJ -- Our client, a leading pharmaceutical company, is currently recruiting a Director of Product Development who will infuse the Product Development Team with their talent, energy and leadership skills. This is an exceptional opportunity to join a corporate culture that is known for its innovative and growth-oriented vision. Assignments include: 1) Develop strategies for products, including technical, regulatory and intellectual property 2) Interact with various teams to ensure timely completion of new product development projects 3) Oversee formulation approaches for analytical method and manufacturing process development 4) Direct and manage batch manufacturing and review and approve technical documents 5) Interact with Manufacturing, Validation and Materials Management to ensure smooth technology transfer and scale-up of formulations to commercial scale 6) Interact with the Regulatory Team to meet CFDA qualifications for smooth registration

Executive Director of Regulatory Affairs (MyBiotechCareer)
Manhattan, NY -- A leading company in the biopharmaceutical industry is currently seeking an Executive Director of Regulatory Affairs to join their team. The role will be challenging but also highly rewarding and this leader will be a key voice in the company. For the right executive, this is a fantastic opportunity with great growth prospects. Key duties include: 1) Develop and implement regulatory affairs strategies and tactical work plans 2) Identify and assess regulatory risks and understand global imperatives, including market-related drivers 3) Keep up with US and global regulatory qualifications and guidance and oversee and review key regulatory documents 4) Present and defend regulatory plans to the Senior Management 5) Lead with preparing and managing timely regulatory submissions 6) Ensure all reporting obligations are met, including amendments, annual reports to FDA, safety and quality reports

Project Manager (MyBiotechCareer)
Franklin Lakes, NJ -- Our client, a leading medical device company, is currently seeking an accomplished Project Manager to join the team. Here is an overview of the role: 1) Lead product development efforts using various processes and tools 2) Ensure the implementation of product development processes and design control procedures 3) Design and execute proper planning, including creation of the project work breakdown structures 4) Lead multiple projects of low to moderate complexity 5) Develop technical and business process solutions to complex problems which require regular use of ingenuity and creativity 6) Follow processes and operational policies 7) Ensure appropriate resources are available for the project 8) Communicate team strategies and plans and execute results at various review meetings 9) Establish and ensure adherence to budgets, schedules, work plans and performance qualifications 10) Participate in product portfolio roadmapping exercises 11) Perform other duties as assigned

Clinical Trial Associate (MyBiotechCareer)
Manhattan, NY -- Our client, a leading biotechnology company, is currently seeking an accomplished Clinical Trial Associate to join the team. Here is an overview of the role: 1) Manage clinical trials emphasizing intensive interaction with study coordinators and data managers at investigational sites 2) Organize specific study related training and study site initiation meetings in close collaboration with the Contract Research Organization 3) Overview all trial related activities such as collection of laboratory test samples, specific sub-study procedures, etc. 4) Ensure that appropriate procedures are in place for the enrollment of patients into the clinical trial 5) Participate in regular conference calls and meetings to review progress of ongoing clinical trials 6) Track and check eCRFs for data correctness 7) Ensure that queries generated during cleaning are responded to on time 8) Confirm that sites are notified and that all company procedures for SAEs are complied with

Project Manager (MyBiotechCareer)
Parsippany, NJ -- A brilliant opportunity exists for an outstanding individual capable of fitting into this very rewarding Project Manager role. Our client, a leading consulting company, is looking to hire someone who can bring added value to the team. If you’re dedicated, energetic and detail-oriented, this could be the perfect role for you. Assignments include: 1) Lead the Project teams and maintain professional relationships with clients 2) Plan, schedule and control project activities to fulfill objectives and project qualifications 3) Develop project plans and align project tactics with project strategies 4) Serve as a Project Advocate within the client's organization 5) Coordinate and motivate all project resources 6) Lead Risk Management within the Project teams 7) Manage projects within established scope, schedule and budget 8) Develop strategies to accomplish specific project objectives 9) Lead project meetings and manage change and conflict


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