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You searched for Biotech Jobs in Washington, DC

Sales Development Representative - Biotech (Dealslister)
Rockville, MD -- Company OverviewCanon BioMedical, Inc. is dedicated to extending innovative Canon core technologies into the burgeoning life sciences field — and to the introduction and marketing of vital, new-platform products in the critical area of molecular diagnostics. Canon U.S.A., Inc., is a leading provider of consumer, business-to-business, and industrial digital imaging solutions to the United States and to Latin America and the Caribbean markets. With approx $29 billion in global revenue, its parent company, Canon Inc. (NYSE:CAJ), ranks 3rd overall in U.S. patents granted in 2016† and is 1 of Fortune Magazine's World's Most Admired Companies in 2016. Canon U.S.A. is committed to the highest level of customer satisfaction and loyalty, providing 100 percent U.S.-based consumer service and support for all of the products it distributes. Canon U.S.A. is dedicated to its Kyosei philosophy of social and environmental responsibility.

Mid Level + Patent Prosecution - Biology / Biotech (The Resumator)
Washington, DC -- Company Overview Law firm's DC office works with a wide spectrum of clients. Job description The perfect applicant will have 5+ years of top law firm background of responding to US Office Actions and drafting high quality U.S. patent applications related to the bio industry. Experienced Patent Associates and Patent Agents welcome to apply. Responsibilities and Duties Patent Drafting The perfect candidate will have background of drafting high quality U.S. patent applications for major technology companies. Patent Office Actions Applicant will have background responding to office actions with the USPTO. Due Diligence, Opinion Matters and Patent Searches. Patent Portfolio Strategy. Integral Member of the Team Law firm invests in attorneys with both mentorship and professional growth. Requirements and Skills Degrees Ideal applicants will have a Biology related advanced degree; PhD preferable. Admissions Firm seeks a applicant eligible for the USPTO; DC Bar if attorney.

Biotech Patent Agent with 1+ year of biology experience (BCG Attorney Search)
Washington, DC -- Washington, D.C. office of our client seeks biotech patent agent with 1+ year of background

Sales: Biotech Patent Agent 19176GP - Arlington, Virginia (LocalJobBoard)
Arlington, VA -- This international general practice firm is seeking a highly motivated and qualified Patent Prosecution Agent with substantive industry background and a Ph.D. in biotechnology to join their busy life science IP group. Duties include but are not limited to: conducting prior art database searches for patentability and freedom to operate analyses; analyzing patent and scientific papers and documents to assist patent attorneys on patent prosecution, counseling, and litigation; drafting patent applications and responses to office actions; and advising lawyers on technology issues in preparation for depositions. The perfect applicant will have superb technical, written and oral communication abilities, as well as a broad scientific knowledge in the chemical arts. This individual must possess initiative, be a fast learner, and work well with others.

Sales: Biotech Patent Agent 19176GP - Columbia, Maryland (LocalJobBoard)
Columbia, MD -- This international general practice firm is seeking a highly motivated and qualified Patent Prosecution Agent with substantive industry background and a Ph.D. in biotechnology to join their busy life science IP group. Duties include but are not limited to: conducting prior art database searches for patentability and freedom to operate analyses; analyzing patent and scientific papers and documents to assist patent attorneys on patent prosecution, counseling, and litigation; drafting patent applications and responses to office actions; and advising lawyers on technology issues in preparation for depositions. The perfect applicant will have superb technical, written and oral communication expertise, as well as a broad scientific knowledge in the chemical arts. This individual must possess initiative, be a fast learner, and work well with others.

Sales: Biotech Patent Agent 19176GP - Washington, DC (LocalJobBoard)
Washington, DC -- This international general practice firm is seeking a highly motivated and qualified Patent Prosecution Agent with substantive industry background and a Ph.D. in biotechnology to join their busy life science IP group. Duties include but are not limited to: conducting prior art database searches for patentability and freedom to operate analyses; analyzing patent and scientific papers and documents to assist patent attorneys on patent prosecution, counseling, and litigation; drafting patent applications and responses to office actions; and advising lawyers on technology issues in preparation for depositions. The perfect applicant will have superb technical, written and spoken communication abilities, as well as a broad scientific knowledge in the chemical arts. This individual must possess initiative, be a fast learner, and work well with others.

Head of Bioanalytical Group - Contract Research Organization - Gaithersburg (The Job Spider)
Gaithersburg, MD -- of the largest biotech hubs in the country. Shall: *** Act as the strategic and scientific lead for the group

Fill Finish Specialist (MyBiotechCareer)
Rockville, MD -- A brilliant opportunity exists for an outstanding individual capable of fitting into this very rewarding Fill Finish Specialist role. Our client, a leading contract research 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) Provide technical support for both government contracts and commercial projects 2) Monitor activities within the class A/B areas 3) Work on various projects and tasks 4) Maintain aseptic process throughout the fill tasks 5) Oversee various operations are in accordance with cGMP guidelines 6) Identify issues and give adequate solutions 7) Review SOPs, batch records, deviations and other technical documents 8) Oversee the inventory of components and its spare parts 9) Comply with GMP regulations 10) Maintain all processing equipment and instruments as per approved procedures

Director of Medical Writing (MyBiotechCareer)
Rockville, MD -- A leading company in the life sciences industry is currently seeking a Director of Medical Writing 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) Manage the clinical document portfolio required for a project and provide creative solutions 2) Write and edit study protocols, reports, other clinical study-related regulatory documents, journal publications, congress presentations and agency presentations 3) Analyze industry trends for study reports and international dossier preparation, including electronic document submissions and synthesize standardized solutions 4) Prepare internal guidelines for document preparation and templates for clinical documents 5) Prepare and implement writing guidelines in compliance with recognized standards 6) Develop strategy for document preparations and document review processes

Clinical Trial Manager (MyBiotechCareer)
Gaithersburg, MD -- Our client, a leading pharmaceutical company, is currently seeking an accomplished Clinical Trial Manager to join the team. Here is an overview of the role: 1) Track and manage the progress of clinical study activities 2) Work with the department leads to maintain projects within intended timelines and project budgets 3) Identify issues affecting study conduct and work with the department leads on a satisfactory resolution 4) Develop requests for proposal and coordinate with the selection of CROs and outside vendors 5) Manage outside vendors and contractors 6) Track key project metrics and action items 7) Oversee the development of study protocols, study timelines and budgets 8) Track vendor and site payments and coordinate the development of documents in support of clinical studies 9) Support site management and monitor efforts, as needed 10) Monitor select sites to ensure protocol & GCP compliance 11) Participate in the development, review and maintenance of clinical operations SOPs

Senior Manager of Regulatory Affairs (MyBiotechCareer)
Gaithersburg, MD -- Our client, a leading biotechnology company, is currently seeking an accomplished Senior Manager of Regulatory Affairs to join the team. Here is an overview of the role: 1) Lead all regulatory activities for the assigned area 2) Develop regulatory strategies for assigned products 3) Prepare regulatory submissions 4) Monitor corporate activities for regulatory compliance 5) Manage and lead the Regulatory Affairs Department 6) Review documentation supporting regulatory applications 7) Lead interactions with regulatory agencies 8) Build professional relationships with project managers and other key personnel, as appropriate 9) Communicate with outside regulatory agencies regarding submissions 10) Perform other duties as assigned

Director of Regulatory Affairs (MyBiotechCareer)
Gaithersburg, MD -- A leading company in the biotechnology industry is currently seeking a 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) Represent Regulatory Affairs at cross-functional teams 2) Plan and execute regulatory filings 3) Review documentation supporting regulatory applications 4) Manage the Regulatory Affairs Department to interface with regulatory authorities in an appropriate manner 5) Manage regulatory activities for the company’s product portfolio 6) Direct the Regulatory Affairs Department in developing and implementing regulatory affairs strategies 7) Establish regulatory positions for new and existing products 8) Participate in labeling and promotional material review processes 9) Prepare and communicate regulatory risk assessment to the Business Unit Team and Senior Management

Senior Director of Regulatory Affairs (MyBiotechCareer)
Gaithersburg, MD -- Our client, a leading biotechnology company, is currently recruiting a Senior Director of Regulatory Affairs who will infuse the Regulatory Affairs 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) Manage the Regulatory Team at various sites 2) Develop and implement a regulatory strategy for vaccines 3) Guide cross-functional groups regarding all aspects of manufacturing, quality, preclinical and clinical testing of products 4) Plan and execute required regulatory filings 5) Prepare the Regulatory Team for health authority meetings 6) Manage the Regulatory Affairs Department to interface with regulatory authorities in an appropriate manner 7) Represent Regulatory Affairs at cross-functional teams 8) Prepare and communicate regulatory risk assessment to the Business Unit Team and Senior Management

Senior Medical Director (MyBiotechCareer)
Linthicum Heights, MD -- A leading company in the life sciences industry is currently seeking a Senior Medical Director 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 cost management and medical quality improvement activities 2) Review activities related to quality assurance and medical services 3) Implement performance improvement initiatives 4) Review complex cases and medical appeals 5) Participate in network provider development and new market expansion, as appropriate 6) Assist with developing and implementing physician education 7) Evaluate adverse trends in utilizing medical services 8) Assist with reducing unwarranted variation in clinical practice 9) Review claims to determine medical necessity and appropriate payment 10) Perform other duties as assigned

Director of Clinical Development (MyBiotechCareer)
Rockville, MD -- A biotechnology company is currently seeking a 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) Oversee the design and implementation of clinical projects 2) Integrate pre-clinical and early clinical findings with planned clinical programs 3) Investigate and track clinical development 4) Prepare clinical development plans and approve clinical protocols 5) Manage cost-effective clinical development programs 6) Implement R&D policies, SOPs and related activities 7) Lead and analyze data evaluation processes 8) Prepare regulatory and other documents for the Regulatory Department and other agencies 9) Manage and delegate tasks to the Clinical Team 10) Perform other duties as assigned

Regulatory Affairs Manager (MyBiotechCareer)
Gaithersburg, MD -- Our client, a leading biotechnology company, is currently seeking an accomplished Regulatory Affairs Manager to join the team. Here is an overview of the role: 1) Oversee regulatory activities for the assigned territory 2) Establish regulatory strategies for assigned vaccine products 3) Prepare regulatory submissions, including annual reports 4) Review and document regulatory applications 5) Provide gap analysis based on regulatory qualifications 6) Plan and coordinate meetings and teleconferences 7) Manage regulatory activities to ensure license compliance 8) Interact with the company’s partners and consultants 9) Track and ensure that regulatory commitments are met 10) Perform other duties as assigned

Manufacturing Director (MyBiotechCareer)
Rockville, MD -- A biotechnology company is currently seeking a Manufacturing Director 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) Analyze production efficiencies, variances and procedures within the department 2) Establish and manage budgets, manpower and other resources within corporate policies 3) Conduct briefings and technical meetings for the Senior Management and customers 4) Develop and implement new and unique methods and procedures 5) Maintain the quality of the technical output and the performance of programs 6) Coordinate and monitor milestones with the customer and the Project Manager 7) Prepare protocols, procedures and specifications, as required 8) Comply with the company’s policies and quality system SOPs 9) Perform other duties as assigned

Controller (MyBiotechCareer)
Clarksville, MD -- Our client, a leading pharmaceutical company, is currently seeking an accomplished Controller to join the team. Here is an overview of the role: 1) Oversee cost and inventory accounting and revenue recognition activities 2) Prepare budget and financial forecasts and report variances 3) Maintain internal controls and safeguards 4) Manage reporting systems and vendor relationships 5) Monitor cash flows, employees’ expenditure and maintain daily and monthly cash reporting systems 6) Review and ensure timely reconciliation of all bank accounts 7) Oversee the preparation and filing of IRS forms 8) Manage the company’s fleet vehicles 9) Monitor the company’s on-line pharmacy, including sales and inventory 10) Coordinate activities with external and internal auditors 11) Prepare and publish monthly financial statements 12) Manage the preparation of regulatory reports 13) Comply with local, state and federal government reports and tax filings

Analytical Laboratory Director (MyBiotechCareer)
Rockville, MD -- Our client, a leading biotechnology company, is currently recruiting an Analytical Laboratory Director who will infuse the Laboratory 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) Establish and manage budgets, manpower and other resources within corporate policies 2) Conduct briefings and technical meetings 3) Comply with cGMP and ICH regulations, standards and guidelines, as required 4) Identify grants or other funding opportunities 5) Evaluate potential funding opportunities and present to the Senior Management 6) Provide direct supervision to the assigned staff 7) Achieve max performance levels and the company’s goals 8) Interview and hire new employees with the help of the HR Department 9) Administer disciplinary actions to the staff, when required 10) Perform other duties as assigned

Regulatory Affairs Specialist (MyBiotechCareer)
Gaithersburg, MD -- Our client, a leading biotechnology company, is looking for a Regulatory Affairs Specialist to join their team. If you have the necessary experience and are up for a challenge, this could be a great opportunity for you. Assignments include: 1) Support product development teams through product life-cycle 2) Provide regulatory assessments to manufacturing, design changes and validation activities 3) Support international product registrations 4) Identify guidance documents and international and consensus standards 5) Assist with product development teams 6) Review and approve product labeling, training materials and advertising and promotional materials 7) Track and maintain regulatory registrations and product blocking lists 8) Ensure international regulatory clearances, sales and commerce implications 9) Use technical and regulatory principles, theories and concepts 10) Negotiate with the FDA and other regulatory agencies 11) Sustain regulatory affairs product files

Director of Financial and Corporate Communications (MyBiotechCareer)
Gaithersburg, MD -- A biotechnology company is currently seeking a Director of Financial and Corporate Communications 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 execute the financial communications plan 2) Plan and coordinate communication aspects 3) Build and maintain vendor relationships 4) Manage corporate web sitecontent and infrastructure 5) Develop finance related scripts and presentations 6) Lead corporate communication projects 7) Coordinate with vendors, budgets and timelines 8) Manage relationships with external design agencies 9) Plan and manage multiple complex projects 10) Perform other duties as assigned

Senior Manager of External Development (MyBiotechCareer)
Gaithersburg, MD -- We are seeking a driven individual with a passion for the biotechnology industry. 1 of our clients is looking to add a strong Senior Manager of External Development to their team. Assignments include: 1) Lead complex proposal submissions 2) Manage and prepare basic and complex proposals 3) Understand proposal qualifications and develop flexible plans 4) Develop and write various proposal sections 5) Work with subject matter experts to prepare written documents 6) Leverage external relationships to gather competitive intelligence 7) Understand competitors’ strength and weaknesses and implicate internal programs 8) Identify business unit growth strategies 9) Develop win themes for complex proposals 10) Lead internal and external meetings with min guidance and support 11) Implement strategies to develop programs with general instructions 12) Develop and execute capture plans 13) Develop and maintain customer relationships 14) Provide updates on customer needs, priorities and budget

Clinical Data Specialist Job (The Job Spider)
Germantown, MD -- Clinical Data Specialist (Germantown, MD) Design, build and manage the biological study data collection modules; Review and validate the clinical data from both Korean and US sites for clinical and biological studies of Korean clients under the FDA’s regulations; Create the guidelines/instructions for the study data collection modules and manage/update the documents per communicating with Korean clients; Identify incomplete and inaccurate parts of collected clinical data and correct discrepancies as communicating with Korean clients; Communicate with Korean laboratory vendors for the lab data management; Develop the specific study documents per Korean client’s comments and manage the documents; Create the general templates/guidelines of clinical/biological data management documents/processes; Work with US and Korean CRAs and site coordinators for the clinical data issues; Translate scientific clinical documents and data in Korean for US clinical trials; 40 hrs/wk.

Sr. Toxicologist - Genotoxicity Job (The Job Spider)
Bethesda, MD -- Lead studies involving advanced modeling, pathology, toxicology and biocompatibility for drug development organization to support applied research for integrated product development. Qualifications: *** Ph.D, MD or OD *** Hands on work experience with animate and inanimate tissue. *** Knowledge of Genetic Toxicolgy Practices, regulations, GLP, ICH, etc.. A highly visible, collaborative senior level position where you will be the backbone of a scientific team for all proposed, active, and completed projects. This role is a key position. As such, employment packages may include executive perquisites as well as company paid family medical, dental, prescription, etc., 401(k), attractive vacation packages, bonus plans, and a starting salary up to $125,000. For full information, confidentially contact Christopher Moreno at: (609) 584-XXXX ext 264 Or submit resume on-line at: http://dmc9.com/cam/app.asp Or email to: XXXX@jobbank303.com Please reference #37158169 when responding.

Regional Medical Specialist *** DC Area*** Job (The Job Spider)
Washington, DC -- The Regional Medical Specialist (RMS) will be responsible for educating across the continuum of healthcare providers on Assurex Health's pharmacogenomic product lines and relevant therapeutic areas. The RMS will develop and maintain internal and external relationships in assigned geographic areas, maintain a high-level of customer service, and demonstrate accountability for their part in the corporate growth. This position will report to the Regional Medical Affairs Manager. • Provide lectures, lead discussion groups, and through phone, internet and other means, educate physicians, other health care professionals, and the sales team about psychiatric pharmacogenomics and therapeutic areas relevant to the company's products • Address daily clinical support questions from health care professionals for all products • Participate in local, regional


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