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- Northern San Jose area, CA

Sr. Systems Engineering Manager-San Jose area CA Our client, a Fortune 150 Global Supplier of Specialty Medical Diagnostic Equipment manufacturer designing and launching next generation platform and accessories is looking for a Sr. Manager Systems Engineering – V&V who will be hands-on and direct the R&D Systems Verification & Validation organization responsible for developing and launching complex electromechanical diagnostic IVD equipment The System Verification & Validation....


Our client, a well-known Provider of Language Services with offices around the world, is seeking an Account Executive for their Life Sciences Translations group. The individual will be based out of the New York office and will be tasked with generating new business in the Life Sciences (Pharma/Med/Bio) space for this provider of translations to over 100 languages. Reporting to the Sr. VP of Global Sales, the Account Executive would be responsible for covering the U.S. We provide a growth path....


Publicly traded Boston based pharmaceutical company is expanding and looking for: experienced Associate Director of Clinical Trial Disclosure and Transparency to lead, define, execute, and efficiently manage clinical trial disclosure and transparency activities. This newly created position will report to the Head of Medical Writing and will be a key player in evaluating, developing, and implementing efficient, quality compliant processes and systems to ensure overall effectiveness. In....


GENERAL DESCRIPTION:This position provides leadership to the manufacturing department engaged in the production of both clinical and commercial drug products. The Associate Director ensures that the production department is adequately staffed with properly trained, knowledgeable employees who perform their duties according to approved Manufacturing directions, Standard Operating Procedures, company guidelines for safety and environmental compliance, as well as current European and US Good....


Process Controls Engineers with DeltaV experience needed for reputable award-winning Automation and Control Systems Integration company. Great chance to use your industrial automation experience within the Biotech, Pharmaceutical, and Food and Beverage industries. Why work here?:Stable business for 25 years and growing!Fun and professional environment with over 120 employees!Variety of projects in several industries, many pharmaceutical and biotech projects!Training provided on new technology....


Global Pharmaceutical company which focuses in Rare Disease, Oncology and Infectious Disease is hiring a Biosmaple Operations Manager Must have GCP experience and Sponsor experience (Biotech or Pharmaceutical) One year w-2 contract with full benefits offered Or can go permanent Full time Send resume if interested and qualified:Company is seeking a Biosample Operations Manager to support the clinical teams and to work across its projects as well as with the external biorepositories, assay....


Global Pharmaceutical company (headquarted in West Palm BEach, Florida) is growing and needs a Strong Clinical Lead (someone who mas managed the CRAs and the clinical study trials but can also monitor when needed as Snr CRA). Snr Clinical Research Associate for oncology trials. Must have five to eight years of experience with at least two years of oncology experience. Must come from a Sponsor company (Pharma or Biotech) and be bi-lingual (spanish speaking - many sites are in Latin America).....


Top Tier Pharmaceutical company (with focus in RESPIRATORY, CNS, Diabetes, Cardio, GI and more) in Madison, NJ is looking for three Clinical Trials Manager Consultants for Clinical Trials Group This is a one year contract and can continue for up to 4 years (1099 or w-2)SummaryParticipate in all aspects of clinical development and study management under the direction of the Director, or designee, which includes providing scientific, and/or logistical support to planned and ongoing trials CTM –....

- Manhattan, NY

As a Study Leader Team Lead/Assistant Director, you will manage and mentor a group of approximately 10 study leaders and associates in order to maximize their capabilities to deliver high quality clinical studies. People Management · Coach and develop global staff to maximize their contribution to the delivery of studies across various therapeutic areas · Manage performance of direct reports through regular dialog and throughout the year in accordance with the Roche performance management....

- Cranford, NJ

Global Pharmaceutical company is hiring a \ for their growing company. Our Clinical Trainer is responsible for identifying and implementing Clinical Development staff training needs. They may benchmark Clinical SOPs and insure SOP training is completed and up to date. The Clinical Operations Trainer may also periodically co-monitor and evaluate staff performance and provide guidance for performance, improvement and adherence to FDA and SOP requirements. They may liaise with US and Taiwan....

- Waltham, MA

Incredibly successful publicly traded Biotech in Waltham , Massachusetts is expanding due to their clinical trial success. Looking for a Strong Clinical Trials Manager or Senior Clinical Trials Manager to help lead their Phase 2 and 3 trials in anti-cancer partner drugs. This company has three wholly owned therapies- in late stages, with a fourth starting in phase I. This CTM is focused on the anti- cancer phase III trials. If you are an experienced Clinical Trials Manager with oncology....


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....


Leading Controls System Integrator specializes in process automation and manufacturing intelligence need to add a Controls Engineer with some manufacturing IT experience to their team due to growth. If you are a Controls Engineer and have an interest in IIOT, Real-time production analytics, or Manufacturing Execution Systems (MES), then this could be ideal for your career. Why work here?:Stable company in business for over 30 yearsVariation of projects in many industries including Biotech,....

- San Diego, CA
new job!

My client seeks to hire a Director of Computational Chemistry -- the ideal candidate is both strategic and tactical. This person will impact the organization with strong drug discovery experience. The Director will have made a significant impact to their current organization and will bring a strategic vision for this group. The ideal candidate will take on the following tasks:Provide effective computational chemistry project support that advances projects against key milestonesDirect external....

- New York, NY

My client is in start-up mode seeks a Director to oversee clinical research and drug safety activities along with clinical research strategy. The ideal candidate will take on the following tasks:Oversee clinical study activities.Recruit, manage and develop a small clinical research and drug safety team.Oversee data analysis, evaluation and reporting of clinical data including study reports, FDA and ethics committee progress/final reports, and assist with manuscript preparation.Forecast....

- Madison, WI

Director - QC Stability & Release Testing (GMP), your basic purpose will be to ensure efficient and effective management. You will supervise and assist group leaders and scientists in laboratory operations with tasks such as scheduling, resource management, technical and compliance related issues. In addition, you will plan, direct and implement improvements in systems, processes and procedures to increase efficiency, productivity and quality in the laboratory. You will assist the division


Director Analytical Method Development & Validation (GMP Biopharmaceutical - PhD preferred or MS with LOTS (5+ mgt, 10+ GMP) - Analytical Method Dev’t, qualification and validation experience required - Complex and New Method work - Large Cell experience is a must - Would love to have protein Characterization and analytics - GMP and STRONG leadership (team up to 60-100), Financial Management


Leading Pharmaceutical Company with marketed products and strong Neurology Pipeline is looking for a Director, Medical Information for their growing US Headquarters in Waltham, MA Competitive Base, Bonus, Long Term Incentives and Relocation The Director, Medical Information (MI) will be responsible for leading the MI function within the Medical Affairs. The Director, Medical Information will be responsible for managing the member of the MI function who are providing and supporting the....

- Palo Alto, CA

The Director, Medical Writing is responsible for the efficient preparation of high-quality, strategically aligned medical writing deliverables that support the clinical development, clinical safety and regulatory requirements of a clinical program. He/she is also responsible for the messaging strategy across a program of work, for the provision of strategic input into the development of development plans and submission plans, and for analyzing proposed plans, programs, individual studies and....

- Palo Alto, CA

The Director is primarily accountable for nonclinical toxicology, working in collaboration with nonclinical pharmacology and pharmacokinetic scientists to drive the overall global nonclinical regulatory submission strategy and coordination for multiple company portfolio products, from research to registration and beyond. The individual has experience in evaluating and responding to inquiries from regulatory authorities addressing global nonclinical development issues in support of IND and....

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