Biotech Meeting Jobs

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Lead project execution after deal closure with ultimate accountability for project initiation, planning, execution and control (cost, time, quality and risk) Direct and motivate multi-disciplinary project teams and keep team members accountable to deliver Conduct internal and external Project Team Meetings to ensure that all stakeholders and the customer are working in accordance to the agreed t...

Regional Account Manager – Northeast – New England States (MA, CT, RI, VT, NH, ME): My client, a well established biotech company situated outside of Boston, has multiple commercialized products and a solid pipeline. They are a company committed to growing their current therapeutic areas as well as entering into new ones such as oncology by developing both biotherapeutic proteins and small molecu...

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Regional Account Manager – Northeast – New England States (MA, CT, RI, VT, NH, ME): My client, a well established biotech company situated outside of Boston, has multiple commercialized products and a solid pipeline. They are a company committed to growing their current therapeutic areas as well as entering into new ones such as oncology by developing both biotherapeutic proteins and small molecu...

Regional Account Manager – Northeast – New England States (MA, CT, RI, VT, NH, ME): My client, a well established biotech company situated outside of Boston, has multiple commercialized products and a solid pipeline. They are a company committed to growing their current therapeutic areas as well as entering into new ones such as oncology by developing both biotherapeutic proteins and small molecu...

RESPONSIBILITIES: Kforce has a client seeking a Project Manager- Medical Device / Biotech in Thousand Oaks, California (CA). Responsibilities: Provide additional PM support to manage Product launch SKU activities and clinical Auto injector supply issues that are occurring in parallel Manage meeting logistics Develop and manage detailed schedules Track deliverable to closure Document and com...

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Pearl Therapeutics The Sr. QC Analyst will support Pearl's Clinical and Commercial Manufacturing Operations by managing day to day operations of EM, MLT and critical utilities testing programs. This position will also provide chemical and physical testing characterization support of APIs and raw materials using established chromatographic and aerosol performance method. Responsibilities · Manag...

WHO WE ARE Watch our story and learn more about Bio-Techne here: http://www.bio-techne.com/our-story POSITION SUMMARY The responsibilities of this position are toassist field sales staff in achieving territory sales goals through interviewing prospects and providing technical information as well as features and benefits on all Biotech product lines. Also assist TSR 2's in general sales duties i...

ORCAS Project Controls is expanding our operations in Southern California. We are looking for a construction Cost Manager who can support a multi-year dynamic program. The construction program will consist of multiple projects ranging from hospitality, office, and labs. Responsibilities  Develop effective cost structure/architecture to manage multiple scopes across multiple organizations and m...

Director of Corporate Development & Training - Biotech / Pharmaceutical Resumes to ***** My client provides a broad array of healthcare marketing solutions, including comprehensive direct-mail, fulfillment, sampling, database, and sales force management for the Pharmaceutical and Healthcare vertical. The Director of Corporate Development and Training is responsible for the effecti...

The individual will be responsible for developing Product Protection solutions and associated processes. Product Protection is defined as the application of security features (overt, covert, forensic) to packaging components and products as well as the application of Tamper Evidence. Specific responsibilities include, but are not limited to: · Support the Product Security technology selection pr...

Regeneron Pharmaceuticals is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, inc...

Regeneron Pharmaceuticals is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, inc...

About The Opportunity:This is a great opportunity for someone looking to join an exciting pharmaceutical company in the greater Philadelphia area. Our client is highly successful and provides a team driven environment. With a strong pipeline and a significant revenue stream, the sky is the limit with this organization.If you enjoy working in a collaborative programming community, this is the perfe...

Ascent Pharma is looking for a Home-based Sr. Clinical Data Manager! RESPONSIBILITIES: •Review protocols for proper data capture including Case Report Form design. Able to perform a thoroughly detailed review of CRF data requirements. •Designs CRFs and creates annotated CRF and CRF completion guidelines. •Develop a Data Management Plan that outlines CRF flow, data queries, manual checks, and d...

Are you looking for your next job opportunity? Are you looking to grow with a well know company in the pharmaceutical industry? Well I have the perfect opportunity. This is a 3 month contract in the Berkeley Heights, NJ area. You may respond by sending an updated resume.Contract Pharmacovigilance Manager: Governance: Monthly Product Safety Review Meetings• Coordinate monthly intra-department mee...

Work with Head, Central Clinical Trial Operations to: Responsible for the operational strategy of assigned clinical trials, including operational planning and execution according to study objectives and adequate preparation and training of teams supporting the study. Leads the cross-functional Clinical Trial Team functions contributing to the relevant clinical trial(s) and relevant vendors to en...

Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include sit...

Looking for a Permanent Manager of Operations based in Philadelphia , San Antonio, TX or Dallas, TX Looking for someone to manage the client relationship and CRAs/Trial Managers based across the US.The person will need to be available to travel and be able to conduct Site Assessment Visits with each CRA managed approximately twice a year. The ideal person should have previously managed CRAs/ cli...

Essential Function The responsibility of a Sr. Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOPs. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when requ...

DOCS is actively seeking a Regional CRA with Oncology experience. May require up to 50% travel. Responsibilities include: -Coordinate monitor, reviews and generate queries of CRF's for clinical trials -Interface with, and assure training of investigators, center staff, trial monitors and clinical staff -Ensure adequate monitoring is conducted on all clinical trials including identification of...