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- North Houston, TX

Location: North Houston, TXImmigration status: our client cannot transfer nor sponsor for any type of visa and you must join them full-time.No Relocation is offered by the Client - Candidate must be willing to Self-Relocate We are currently looking for a Medical Operations Analyst for a highly rated Healthcare organization. This person will need to have an extensive knowledge of health care terminology and standard coding systems along with the experience of working within an analytic or....


Position: Project Manager – Cardio / Sleep Apnea Locations: Atlanta, GA Scope of Patient Flow – Project Manager The Patient Flow Manager is a Project Manager responsible for the successful planning and execution of projects as assigned by the Chief Operating Officer. Projects will range in complexity and could involve a diverse set of components with cross functional departments for the key operational initiatives of the company. Projects will include working with the company Sales team,....


TITLE: RN Clinical Applications Manager LOCATION: close to Zanesville Ohio Are you looking for a new position where you can live and work in a community that was voted as one of Ohio's Best Hometowns. Would you be interested in working for a healthcare leader in the region? Would you like be in a position of high visibility in the facility where you make a difference? This facility is nestled in the foothills of the Appalachian Mountains and at the intersection of two Interstates that allows....


Well established international contract research organization serving both commercial as well as government markets, is conducting a search for a full time Clinical Project Manager. This position has remote flexibility reporting to the company's headquarters in Princeton NJ. Responsibilities:Oversees assigned studies and accountable for results for all components of studyReviews and provides input to new project proposals/contract developmentManages and tracks project conduct inclusive of site


Senior Clinical Data Manager, CDM - San Francisco Bay Area Responsibilities: Oversee clinical development activities and strategy executionsing the highest standards, manage the CD plan and the collection and interpretation of clinical dataContribute to the data preparation for reporting study results, regulatory submissions, and publicationsUse EDC Systems for data managementApprise management and project teams of clinical data activitiesContribute to the development and implementation of....


Top Tier Global Pharmaceutical company is expanding and has a need for three Principal (and Senior Principal) Medical Writers for their regulatory submissions. These are Full-time-employee positions- WORK FROM HOME- with strong compensation including full health, stock, bonus, long term and short term incentives and much more! This publicly traded global company is in a huge growth mode! Company plc (NYSE:XXX) is a bold, global pharmaceutical company and a leader in a new industry model –....

- Jersey City, NJ

Top Tier Pharmaceutical company in Jersey City, NJ needs a Senior Document Publisher- for aconsulting project (6 months and then up for renewal - can be 1099 or w-2 with benefits including health and PTO contract renewals up to 4 years- can go perm in future as well - contributes to the strategic planning and preparation of regulatory submissions and supports the formatting, organization, and structuring of major regulatory submissions for his/her assigned products and/or therapeutic area(s)....


Top Tier Global Pharmaceutical company is expanding – Looking for a Director, Clinical Devlopment in their New Jersey office (Jersey City or Madison, NJ) – Supporting their GI programs (Phase III Diabetic Gastroparisis); role will sit in JC for the short term. (Ultimately Madison, NJ). The role will require a MD (GI preferred not required) Must have GI clinical development experience (4-5 years will be sufficient) Will lead and develop Phase III GI program This will be an exciting opportunity....


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....

- Boston, MA

A terrific opportunity to provide leadership and guidance as the statistical expert on a project team within a therapeutic area for a Fortune 100 Drug development company. You will be accountable for all statistical aspects of clinical studies and submissions, including quality, relevance to regulatory perspective, and scientific validity. You will act as key statistical consultant within company. Additional Responsibilities will include project staffing, resource planning and allocation,....

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