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My client is expanding their team and they look to hire a Manager of Business Development to better serve their new and existing clients. This is a great opportunity for a Scientist to go from the bench to the business side. The ideal candidate will take on the following tasks:Work closely with the Director of Business Development and assist with selling services to pharmaceutical and biotechnology clientsUnderstand the drug development needs of the clients and positively position the firm as....


My client is expanding their team and they look to hire a Manager of Business Development to better serve their new and existing clients. This is a great opportunity for a Scientist to go from the bench to the business side. The ideal candidate will take on the following tasks:Work closely with the Director of Business Development and assist with selling services to pharmaceutical and biotechnology clientsUnderstand the drug development needs of the clients and positively position the firm as....

- Somerville, NJ

Our client - a growing Pharmaceutical company in central NJ - is looking for a Clinical Operations Manager. The Clinical Operations Manager will be responsible for the planning and execution of clinical trials. The Clinical Operations Manager will: Lead the study team in order to develop the study planHelp select the CROReview study feasibility assessmentsHelp oversee site selection/site qualificationOversee the management of the logistics of clinical material The qualified candidate will have


Top tier Pharmaceutical company (one n Boston and one in NJ nd one in Seattle)Required:Has completed management of a study or group of studies from planning through close out (Phase 3)Experience with managing VendorsExperience working on global studies with CROs Nice to Have:Experience supporting writing clinical study reports,Supporting sNDA or NDA submissions, Supporting pre-Inspection preparation,Participating in Sponsor Inspections by Regulatory BodiesExperience managing or leading teams....

- Cambridge, MA

My client seeks an outstanding scientist to contribute to drug discovery and development projects. The ideal candidate will work closely with medicinal chemists and other scientists – and apply methods to improve drug properties and efficacy. In addition, this person will apply and develop cutting-edge techniques and interpret data using modeling and data mining. Finally, the ideal candidate will possess leadership qualities to direct projects and collaborations. The level of the position is....


Job Description: We are seeking an experienced and determined professional with a passion for Project Management. As a consultant you will primarily work with clients in the pharmaceutical industry. You will engage directly with key decision makers and have the potential to create true impact. Tasks will mainly relate to Project Management of or within large investment projects. We are looking for a candidate with strong leadership and communication skills who is driven by a desire for....

- Marlborough, MA

Top tier Pharmaceutical and Chemical Company in Marlborough, MA is expanding a 6 month full time w-2 contract with benefits (can be renewed up to 4 years) is looking to hire a Data Quality Facilitator This position is responsible for maintaining and/or creating customer contact data content in accordance with established guidelines within Hologic systems. The Facilitator is responsible for supporting the data quality strategy which is to ensure data integrity through data governance. The....


My client is expanding and looking to hire a Director for their Medical Affairs group. The ideal candidate will take on the following responsibilities:Direct collaborations with academic, pharma and biotech partners and facilitate work with biotech Directors and VPs, academic PIs, and others.Understand the research and drug development needs of existing partners and ensure exceptional service.Develop and expand research and clinical collaborations with new partners. The ideal candidate will....


My client is expanding and looking to hire a Director for their Medical Affairs group. The ideal candidate will take on the following responsibilities:Direct collaborations with academic, pharma and biotech partners and facilitate work with biotech Directors and VPs, academic PIs, and others.Understand the research and drug development needs of existing partners and ensure exceptional service.Develop and expand research and clinical collaborations with new partners. The ideal candidate will....


My client is expanding and looking to hire a Director for their Medical Affairs group. The ideal candidate will take on the following responsibilities:Direct collaborations with academic, pharma and biotech partners and facilitate work with biotech Directors and VPs, academic PIs, and others.Understand the research and drug development needs of existing partners and ensure exceptional service.Develop and expand research and clinical collaborations with new partners. The ideal candidate will....


Top Tier Progressive Bio Pharmaceutical company with offices in Seattle and San Francisco is expanding They are looking to hire a Director of Regulatory Advertising and Promo Description Company rates #1 in Northwest! They are a clinical-stage company developing novel cellular immunotherapies based on two distinct and complementary platforms – Chimeric Antigen Receptors (CARs) and T Cell Receptors (TCRs) technologies. Our goal is to revolutionize medicine by re-engaging the body’s immune....


Position: Gastroenterology Hospitalist Location: Tucson, AZ Our client is seeking a Gastroenterology Hospitalist to join their established practice in beautiful Tucson, Arizona. Physicians can expect to enter a practice with high patient demand and a loyal patient base, in an expanding suburban market. The culture is one that values open communication and feedback from its physicians. Preferred candidate will have three (3) to five (5) years' experience and be BE/BC. Also, will consider new....


Our client - a growing Pharma company - is looking for a Head of Quality for their site located in the Louisville, KY area.The Head of Quality will be responsible for oversight of all QA and QC activities at the site.They will have responsibility for implementing, improving and maintaining Quality Systems (i.e. CAPA, Investigations, Change Control etc.), as well as reviewing and approving all validation and technical reports.Additionally, the Head of Quality will be the primary point of....


ID 1230 R&D Scientist - Pharmaceuticals -- injectables or semisolid exp Location Arlington Heights, IL Summary This role will provide technical expertise for process development to expand manufacturing processes and will aid pilot scale to commercial batches. DutiesConduct pilot scale batchesSupport launch batchesPrepare protocols for verification batchesAssemble proper reports and prepare presentations RequirementsBS Degree, Masters preferred5+ years of industry experienceExperience....


The Lead Control Systems engineer is responsible for control systems design, specification, programming, simulation and testing, and start-up assistance. Often, this person will be the project technical lead and may be responsible for some project management activities. Design responsibilities include requirements definition, functional and detailed design documentation development. Testing responsibilities include factory and site acceptance test development and execution. Programming....

- Cincinnati, OH

The holder of this position is charged with leading effort to prove control of the critical aspects of company operations, whether these relate to process, cleaning, equipment, utilities, computers or other elements. Subject matter expert in at least two main area of validation ( Process/Cleaning/Equipment /Utilities /Facilities/Computer Systems)Lead and structure scientific debate and assessment with peers from other technical areas to develop scientific understandingDetermine levels of....


This position provides technical leadership and accountability for computer system validation and ensures compliance with internal and external computerized system policies and regulations. As the Subject Matter Expert, this individual will ensure sites are fundamentally aware of and proactively implement current computerized system validation practices with particular focus on impact to patient safety, product quality and record integrity. Position scope includes local and global site systems


Top tier growing Global Pharmaceutical company is looking for a vibrant and sharp Manager of Regulatory Affairs to join their dynamic Team The is company has been named top new Pharma and one of the Best Employers in 2017 The role canbe in EITHER their Seattle, WA HQ or their NEW offices in San Francisco (full relocation package offered- And great benefits too) Must be a self starter with initiative and Regulatory Affairs experience in the Pharma industry- must have Regulatory affairs and CMC....

- San Francisco, CA

Our client in the San Francisco Bay area, has a new opportunity for Medical Director with expertise in Oncology NGS. This is a full-time, onsite position, with the opportunity to make an impact, company is seeking a driver to lead change. Medical Director, Oncology NGS San Francisco Bay AreaServes as company’s internal and external oncology / medical expert collaborating with several departments / business units including marketing, market access, salesRespond to questions from physicians and....

- Any US State

Our client needs a doctor with experience in oncology clinical drug development to serve as a medical monitor. Work is estimated to take 10 hours per week to start.RequirementsMedical Doctorate (MD) or equivalent5 years clinical drug development experience in oncologyPhase 1 and phase 2 studiesResponsibilities1. Available to clinical investigator sites as a go-to person in the US for checking eligibility2. Be responsible for interacting with sites on safety management of the study. This will....

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