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1000+ R & D jobs found on Monster.

Jobs 141 to 160 of 30335
Description: We're changing the way health care works for the better. That means consulting with our members, partnering with our physicians, and delivering drugs in the most efficient and effective way. Join us and start doing your life's best work.(sm) We are currently looking for a Principal Statistician to join our team in either Eden Prairie or Minneapolis, MN. This position could also be t...
IT’S MORE THAN A DESK JOB! If you are a graduate of a four-year college or university and are interested in a career that includes service to your country, science, and adventure, you will find a unique opportunity in the NOAA Commissioned Officer Corps (NOAA Corps). The NOAA Corps is the uniformed component of the National Oceanic and Atmospheric Administration (NOAA), a Bureau of the Department...
Great perm opportunity for a Regulatory Affairs Specialistto move to the next level. Great Benefits Location-Princeton NJ 1. Responsiblefor the coordination and preparation of document packages for regulatorysubmissions to ensure the timely preparation of organized and scientificallyvalid submissions including 510(k), INDs, IDEs, NDAs, BLAs and other FDAfilings. 2. Reviewscompany and contractor...
The Quality Assurance Lead III reports to the AssociateDirector, and has responsibility for the support of the Quality function to theneeds of the Compliance Program. 10 month contract. The QA Lead III performs all necessary Qualityand cGMP compliance activities assigned to the team (FEU, OR, or PV) per theneeds of the schedule. The QA Lead III performs quality oversight activitiesfor the deliver...
Senior Manager or Associate Director, Regulatory Affairs-VeterinaryBiological New Projects Successful candidate has expertise in Veterinary Biological productdevelopment to provide leadership within the Biological New Projects team (USand global) and to other projects, as assigned. • Leadthe strategic planning process to define and resolve regulatory issues andimplement regulatory team strategie...
The Judge Group is seeking a Sr. Computer Systems Technologisyt. Primary responsibility will be to provide daily system administration support to the various programs. Candidate will design, build and maintain heterogeneous LINUX / Windows computing environments consisting of workstations and servers, data storage technologies and data back-up infrastructure. Must hold active secret clearance. Ot...
A leading science-based biopharmaceutical company seeks a ManagerCMC Project Management for a permanent opportunity. ***Title level (Associate Manager, Manager, or SeniorManager) will be determined based on skills and experience. Summary: Usingstrong CMC Project Management knowledge, the PM leads the CMC Project team anddrives the assigned CMC Projects with moderate to advanced complexity tocomp...
Our client is seeking an Associate Director, Medical Science Liaison (MSL) for a new six member field-based team. Residing in the Medical Affairs Department and working with cross-functional teams, the MSL will apply scientific experience, knowledge, and skills to execute against strategic plans for emerging customers, including integrated delivery networks. Responsibilities include establishing...
Our client is seeking an Associate Director, Medical Science Liaison (MSL) for a new six member field-based team. Residing in the Medical Affairs Department and working with cross-functional teams, the MSL will apply scientific experience, knowledge, and skills to execute against strategic plans for emerging customers, including integrated delivery networks. Responsibilities include establishing...
Leading pharma client seeks a Global Brand Medical Directorfor a 6 month contract. Medical Affairs leader for assigned compound(s) and /orproject(s under the leadership of a Sr. GBMD or GMA Franchise head. Duties: · For assigned compound/indications, workcollaboratively across functions, within GPT to execute an integrated MedicalAffairs plan including clinical trials, publication, medical educ...
Our client is currently seeking a Contract Medical Writer. SUMMARY OF POSITION The Contract Medical Writer will focus on the preparation, assembly, writing, and review of the analyses and documentation needed in support of clinical trials and corresponding submissions to regulatory authorities. MAJOR ACTIVITIES AND RESPONSIBILITIES Responsibilities may include but are not limited to: • Assist ...
Associate Global Program Medical Director-Immunology 6 month contract The Associate Global Program Medical Director (Assoc.GPMD) is responsible for the scientific and medical strategy of assigned sections of a complex clinical development program (e.g., an indication, new formulation, or specific development phase) or may lead programs of low complexity. Responsible as the leader of the section...
The Contract Senior Clinical Site Manager will be responsible for implementing and executing clinical trials in the sites assigned under his/her responsibility. He/she should ensure compliance with international guidelines, local regulations and corporate policies and procedures. 3 yr contract 60% travel required. Currently working in a regional position from an established home office. Ophtha...
Judge Healthcare is currently hiring a Recruitment Coordinator In Boston, MA. This job will have the following responsibilities: Assists recruiters with scheduling candidate interviews Refers applicants to specific position openings Administers pre-employment forms and tests Checks references and process changes in employee status Qualifications & Requirements: Experience managing/organizin...
Our client is currently seeking a Clinical Project Manager. This job will have the following responsibilities: Manage and develop project team. Supervise and evaluate assigned project staff activities and job performance. Provide continuous support of monitoring responsibilities. Develop protocol monitoring guidelines and other assorted project-specific training instructions. Act as principl...
The Contract Senior Clinical Site Manager will be responsible for implementing and executing clinical trials in the sites assigned under his/her responsibility. He/she should ensure compliance with international guidelines, local regulations and corporate policies and procedures. 9 month contract 60% travel required. Currently working in a regional position from an established home office. Oph...
Leading pharma client seeks an Expert Clinical Manager for a 6 month contract. Responsible for operational aspects of one or more clinical trials (phase I-IV, Expanded Access, Investigator Initiated, registries and Compassionate Use) under the leadership of the CTH. Support all scientific aspects of clinical trial(s) as assigned. Responsible for program level activities as assigned with an entrep...
Dynamic, growing pharma client currently seeking a Senior Project Manager, Clinical Operations. Summary: This position is primarily responsible for implementing clinical studies. Summary of Qualifications: Phase 3 or large Phase 2 experience preferred, Phase 1 experience a plus. Knowledge of clinical trial processes (study start-up to study close-down), GCP/ICH and FDA guidelines, Previous ve...
The Safety Surveillance Team Leader serves as a pharmacovigilance resource for the generation and analysis of potential safety signals for investigational and marketed products within a therapeutic area. The Team Leader supports the Patient Safety Physician in maintaining accurate safety profiles of products within that area, manages the Safety Surveillance Groups aligned with key products or prod...
Leading pharma client seeks: Medical Affairs Leader, Oncology Global Medical Affairs Location: MD or DE. 6 month contract Provide medical expertise and insight into the development and optimization of global brand development and strategy and integrated Medical Affairs Plan, driving its effective and appropriate medical translation out into the regions and markets. In addition the role interfa...

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