Contact info: (866) 371-0687, info@mmsgrouponline.com
181-195 of 195 results
Sort By


CONFIGURATION MANAGEMENT SOFTWARE ENGINEER (SR ) - TS/SCI CLEARANCE (ts/sci ) Dulles VA REQUIREMENTSCurrent and active TS/SCI ClearanceMust be a US CitizenStrong Applications Configuration Management expertiseStrong experience working with GIT or other Configuration management tools2+ years of Application Development experience working with any of the technologies listed below:Operating Systems: Linux, Windows, Unix, VxWorks, QNX, IRIX, Solaris, MQX Programming Languages: C, C++,....


The Medical Science Liaison (MSL) plays a crucial role in Medical Affairs, being part of an exclusive field-based team of medical scientific experts that partner with national, regional, and local key opinion leaders (KOLs). Thus, the MSL has significant responsibility and is expected to provide in-depth scientific, clinical and educational support to KOLs, as well as to internal clinical, sales and marketing teams. In addition, the MSL provides scientific insights back to Medical Affairs....


The Medical Science Liaison (MSL) plays a crucial role in Medical Affairs, being part of an exclusive field-based team of medical scientific experts that partner with national, regional, and local key opinion leaders (KOLs). Thus, the MSL has significant responsibility and is expected to provide in-depth scientific, clinical and educational support to KOLs, as well as to internal clinical, sales and marketing teams. In addition, the MSL provides scientific insights back to Medical Affairs....

- San Francisco, CA

The Medical Science Liaison (MSL) plays a crucial role in Medical Affairs, being part of an exclusive field-based team of medical scientific experts that partner with national, regional, and local key opinion leaders (KOLs). Thus, the MSL has significant responsibility and is expected to provide in-depth scientific, clinical and educational support to KOLs, as well as to internal clinical, sales and marketing teams. In addition, the MSL provides scientific insights back to Medical Affairs....


Senior PD Application & Technology SpecialistImmediate need in an ideal North New Jersey location for a Senior PD Application & Technology Specialist with Savory formulation experience. Ideal candidate will have the following credentials:Apply principles of culinary arts and science to develop the formulas, processing procedures and temperature parameters of flavor key products; such as USDA meat and poultry flavors (regular & organic), vegetable flavors (natural/non-GMO &....


The Manager, Medical Information will assist in the operational oversight of medical information within the Medical Affairs function under the guidance of the Lead of Medical Information. The manager will be responsible for providing and supporting the provision of accurate, scientifically balanced and timely responses to inquiries received from health care professionals, consumers and other customers. The manager will monitor the scientific literature and communicate new data to relevant....


Safety Physician POSITION OBJECTIVE: Supports the Pharmacovigilance team in reviewing, querying, documenting and reporting on all serious adverse events (SAE) & Suspected Unexpected Serious Adverse Reactions (SUSAR) cases related to clinical studies. Essential Job Functions/ResponsibilitiesProvide timely and sound medical review of individual case safety reports (ICSR) from clinical trials.Actively participates in the case initiation process (case triage) and case data inputting/data entry

- Cranford, NJ

As a Clinical Study Monitor, you will work within a clinical team setting to ensure study compliance with protocol, FDA and ICH guidelines. Essential Job Functions/Responsibilities · Ensure the Sponsor, Investigator, and study team adhere to current FDA regulations, applicable ICH/GCP guidelines, local policies and standard operating procedures. · Adhere to monitoring plan protocols; e.g. monitoring visit type, frequency, and required critical monitoring activities by utilizing monitoring....

- Cranford, NJ

Senior Clinical Research Associate POSITION OBJECTIVE: Work within a clinical team setting to ensure compliance with protocol and overall clinical objectives. . Essential Job Functions/ResponsibilitiesParticipates in the preparation and/or review of draft protocol and informed consent documentsPossesses detailed knowledge of the study protocol and its associated activities and timelinesParticipates in conference calls, prepares agenda and summariesCoordinates with project team and other study....


POSITION OBJECTIVE: Provide accurate, efficient and effective programming solutions required for clinical trial analysis and reporting. Perform a wide range of activities that include: understanding study protocols, study designs and SAP; creation of complex datasets, tables, listings and figures using SAS; follow and validate CDISC standards; perform basic quality-checklist code reviews; develop standardized programs to automate routine tasks; design, write and debug macro routines.....


Buffalo, NY, United States Full TimePOSITION OBJECTIVE: Provide accurate, efficient and effective programming solutions required for clinical trial analysis and reporting. Perform a wide range of activities that include: understanding study protocols, study designs and SAP; creation of complex datasets, tables, listings and figures using SAS; follow and validate CDISC standards; perform basic quality-checklist code reviews; develop standardized programs to automate routine tasks; design, write

- Cranford, NJ

Cranford, NJ, United States Full TimePOSITION OBJECTIVE: Work within a clinical team setting to ensure compliance with protocol and overall clinical objectives. This position is based in Client's Cranford, New Jersey office. Essential Job Functions/ResponsibilitiesParticipates in the preparation and/or review of draft protocol and informed consent documentsPossesses detailed knowledge of the study protocol and its associated activities and timelinesParticipates in conference calls,....


Job Type: W-2 contractDuration: 11 monthsLocation: New Haven, CT Position SummaryOur client is seeing an experienced Purification Associate - Biologics Process Development who will conduct experimental studies to develop, optimize and characterize manufacturing processes for biotherapeutic candidates. Other duties include:Execute experimental studies to support scale up of manufacturing processes or troubleshooting of issues at manufacturing scale as required for therapeutic proteinsDocuments....


Seeking a lead environmental scientist for a university in the Dallas, Texas area. This person must be strong at grant funding with strong past experience at creating packets, winning, and managing funding. Prefer a person from water area, possibly disaster water management research. Must have phd degree in environmental research or similar degreees. Must have strong environmental research expereince. This is a true research position - not a teaching or administration role.

- Fremont, CA

Clinical Psychologist – Fremont, CA We have a full-time permanent opportunity for a Clinical Psychologist working for a Federally Qualified Healthcare Center located in Fremont, CA. This position will be working with the underserved population which includes mental health/substance abuse services to underinsured and uninsured populations. Practice:Outpatient OnlyEmployed Position with a large system in Northern CA Relocation Paid MalpracticeFull Benefits (Life, Health, Dental and 401k) Good....

181-195 of 195 results