better Biotech Pharma Job in Maryland

DUTIES AND RESPONSIBILITIES: Tasks related to implementation of epidemiology studies and clinical trials: - Assumes responsibility to ensure ICH/GCP compliance of study conduct and data integrity. - Assists in establishing study time lines, and ensures activities are conducted in order to maintain time lines. - Anticipates issues that could impact on study progress and takes action to avoid or solve them. - Participates/leads discussions and meetings with clinical development personnel, other personnel and collaborators

Our client in Frederick, MD develops and delivers Vaccines and related products and are an experienced in the advanced development of bio defense biologics, including live attenuated vaccines, recombinant vaccines, therapeutics, therapeutic polyclonal antibodies, and alternative vaccine delivery systems. Job Duties: CRA performing in-house duties including... -Assisting clinical project manager(s) in the management and coordination of assigned clinical research studies, in compliance with FDA regulations, ICH

A pharmaceutical company has an opening for an In House Clinical Research Associate in Beltsville Maryland...

POSITION SUMMARY: The Clinical Data Manager is responsible for processing and reviewing data for all clinical trials. ESSENTIAL DUTIES AND RESPONSIBILITIES: - Coordinate the printing, shipping and receipt of CRFs in multiple studies/sites/countries. - Process, review, and query clinical trial data using Oracle Clinical database. - Generate, track, and resolve data queries using data clarification forms (DCFs). - Perform review of CRFs, issue manual queries as needed, and maintain archiving of CRFs in house

In House Clinical Research Associate in Beltsville Maryland...

ESSENTIAL DUTIES AND RESPONSIBILITIES: Implementation and Management of Clinical Trials -Assumes responsibility to ensure ICH/GCP compliance of study conduct and data integrity. -Develops and administers study time lines and budgets, and ensures activities are conducted in order to achieve scheduled milestones and goals. -Anticipates issues that could impact on study progress and takes action to avoid or solve them. -Participates/leads discussions and meetings with clinical development personnel, other company

DUTIES AND RESPONSIBILITIES: The selected candidate will independently and accurately review Case Report Form data for completeness, accuracy, and consistency in accordance with all applicable procedures, will be responsible for performing Quality Reviews and identifying data discrepancies in the clinical data via computerized edits as well as manual checks/listings and appropriately address all issues. In this role you will independently and accurately generate data queries to resolve data discrepancies, prepare

pharmacy experience a significant plus CERTIFICATIONS LICENSURE Maryland pharmacist license required COMMUNICATION SKILLS Must be...

SUMMARY: - Assists in the management and implementation of study protocols - Coordinating development of study materials and plans - Support Clinical project Manager RESPONSIBILITIES: - Performs essential documentation collection, review, and maintenance - Study tracking - Liaises with internal and external partners *MUST HAVE A BACHELORS DEGREE *MUST HAVE RECENT INDUSRTY EXPERIENCE (leading Pharma/Biotech/CRO) 3-5 years Join Aerotek Scientific LLC(SM), one of the fastest growing providers of scientific and

Position Title Biostatistician Location Maryland Bethesda NIH MD04 Clearance Required Yes Clearance...

Job Classification: Direct Hire Description: Our client in Frederick, MD develops and delivers Vaccines and related products and are an experienced in the advanced development of bio defense biologics, including live attenuated vaccines, recombinant vaccines, therapeutics, therapeutic polyclonal antibodies, and alternative vaccine delivery systems. Job Duties: CRA performing in-house duties including... -Assisting clinical project manager(s) in the management and coordination of assigned clinical research

Job Classification: Direct Hire Description: SUMMARY: - Assists in the management and implementation of study protocols - Coordinating development of study materials and plans - Support Clinical project Manager RESPONSIBILITIES: - Performs essential documentation collection, review, and maintenance - Study tracking - Liaises with internal and external partners *MUST HAVE A BACHELORS DEGREE *MUST HAVE RECENT INDUSRTY EXPERIENCE (leading Pharma/Biotech/CRO) 3-5 years Join Aerotek Scientific LLCSM, one

Job Classification: Direct Hire Description: ESSENTIAL DUTIES AND RESPONSIBILITIES: Implementation and Management of Clinical Trials -Assumes responsibility to ensure ICH/GCP compliance of study conduct and data integrity. -Develops and administers study time lines and budgets, and ensures activities are conducted in order to achieve scheduled milestones and goals. -Anticipates issues that could impact on study progress and takes action to avoid or solve them. -Participates/leads discussions and meetings

Clinical Research Coordinator CRC in Maryland Job Location South Baltimore Maryland Category Clin...

Project Manager Clinical Research Permanent jobs Job Location Gaithersburg area Maryland Category Clin...

Clinical Pharmacist Department: Pharmacy Schedule: Full-Time Shift: Day shift Hours: Monday - Friday, Days and every 8th weekend Job Details: Clinical Pharmacy Practitioner Practice or research specialty/focus of the position:Pain Management Position Description:UnionMemorialHospitalis recruiting a highly motivated Clinical Specialty Pharmacist to provide pharmaceutical care for the Pain Medicine Service. The pharmacist will participate in therapeutic drug monitoring and medication management activities. This

accredited School of Pharmacy and a current Maryland pharmacist license...

Clinical Project Manager Frederick Maryland Return to Search Results Send job to...

At PharmAthene, our commitment is reflected in all that we do. We are a company driven by the desire to make a difference and recognize that our success depends on the creativity, dedication and performance of our team. PharmAthene s primary objective is the development of effective countermeasures to a range of potential biological and chemical weapons. We aim to recruit talented scientists and management to lead its programs and oversee the outsourcing of various program activities with an urgency to

Clinical Project Manager Major Duties and Responsibilities (including supervising others): Position Summary: Project Manager is responsible for project and team management for multiple clinical trial projects, either individually or within specific customer programs. These responsibilities include: serving as primary project contact for designated customers; ensuring that project timelines and budgets are agreed and achieved; coordinating project communications to customers; developing, maintaining

Protection Branch and is located in Frederick Maryland...

Clinical Project Manager I 130227 (NCI) Full Time Regular posted 10/3/2008 Job Category CTR - Clinical/Regulatory Req ID 130227 Able to obtain security clearance? None Currently possess security clearance? None Location Bethesda, MD % Travel Relocation Yes Requirements Responsible for management and coordination of assigned activities for the Institutional Review Board (IRB) in support of the Division of Clinical Research (DCR), National Institute of Allergy and Infectious Diseases (NIAID

accredited School of Pharmacy and a current Maryland pharmacist license...

LICENSURE CERTIFICATION Current Maryland Registered Pharmacist license...

Kforce is currently seeking a Clinical Data Coordinator (CDC) for a position in Rockville, MD. The CDC will be responsible for assisting with the day-to-day data management tasks conducted for assigned projects. The CDC provides input into the development of Project Specific CRFs, departmental SOPs, and process improvements, and may participate the training of other CDCs. The incumbent will also participate in study set-up and lock, annotating CRFs, query management, and discrepancy management. Additionally

The EMMES Corporation is seeking a full-time Biostatistician to work in its Rockville, MD office. Primary Responsibilities Collaborate on protocol development. Collaborate with study investigators (clients) on writing manuscripts and abstracts for dissemination of study results. Review protocol design. Conduct sample size and power calculations. Conduct statistical programming to produce monitoring and data management reports. Conduct statistical

Title: Biostatistics Intern Location: Gaithersburg, MD Req: 01218 Major Duties and Responsibilities (including supervising others): The Biostatistics student intern will have three sets of duties: (1) an assigned project requiring an oral presentation of 15 minutes at the termination of the internship period (approximately 3 months); (2) following his/her mentor as a job shadow at various statistical consulting opportunities with Biostatistics business partners; (3) administrative responsibilities, including

Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC) ensures full integration of development and commercialization activities, from initiation of the clinical program for a compound through product positioning and global life cycle management, which will lead to globally consistent branding of our products. Otsuka is seeking a Senior Clinical Programmer/Clinical Programmer for our Rockville MD and Princeton, NJ offices, who will contribute to the development of SAS programs in support of clinical

POSITION SUMMARY: The Clinical Data Manager is responsible for processing and reviewing data for all company clinical trials. ESSENTIAL DUTIES AND RESPONSIBILITIES: Coordinate the receipt of CRFs from multiple study sites/countries Process, review, and query clinical trial data using Oracle Clinical database Generate, track, and resolve data queries using data clarification forms (DCFs) Design CRFs and ensure that all protocol-specified endpoints are appropriately captured Ensure proper archiving of

The Lister Hill National Center for Biomedical Communications (LHNCBC) of the National Library of Medicine (NLM) is developing new tools and solutions that will facilitate patient-centric care, clinical research, and public health. These tools will solve the problem of tracking medication, needed preventive care, important laboratory tests and easily link to NLM s many rich resources of consumer-health databases. Specifically, this position will focus on research and development of open source tools and systems

Job Classification: Direct Hire Description: POSITION SUMMARY: The Clinical Data Manager is responsible for processing and reviewing data for all clinical trials. ESSENTIAL DUTIES AND RESPONSIBILITIES: -Coordinate the printing, shipping and receipt of CRFs in multiple studies/sites/countries. -Process, review, and query clinical trial data using Oracle Clinical database. -Generate, track, and resolve data queries using data clarification forms (DCFs). -Perform review of CRFs, issue manual queries as

Job Classification: Contract Description: DUTIES AND RESPONSIBILITIES: The selected candidate will independently and accurately review Case Report Form data for completeness, accuracy, and consistency in accordance with all applicable procedures, will be responsible for performing Quality Reviews and identifying data discrepancies in the clinical data via computerized edits as well as manual checks/listings and appropriately address all issues. In this role you will independently and accurately generate

Title: Controls Engineer Location: Frederick, MD Req: 01219 Position Summary: Responsible for engineering support of existing and future control systems in a GMP environment to support operations in a manufacturing facility Essential Job Functions:Responsible for engineering support of control systems used for GMP manufacturing processes, utility control systems to support manufacturing, and building control systems. This position will aid with the trouble shooting of control problems. Develop projects for

Title:Director, Clinical Development (Inflammatory) Location: Gaithersburg, MD Req: 01217 Major Duties and Responsibilities (including supervising others): 1. Establish and approve scientific methods for design and implementation of applicable clinical protocols, data collection systems, and final reports. 2. Collaborate with Translational Science to optimize approach to study target neutralization and understand mechanism of action of products. 3. Supervise project team members in planning, conducting and

POSITION SUMMARY: The Clinical Data Manager is responsible for processing and reviewing data for all company clinical trials. ESSENTIAL DUTIES AND RESPONSIBILITIES: Coordinate the receipt of CRFs from multiple study sites/countries Process, review, and query clinical trial data using Oracle Clinical database Generate, track, and resolve data queries using data clarification forms (DCFs) Design CRFs and ensure that all protocol-specified endpoints are appropriately captured Ensure proper archiving

Description: The Lister Hill National Center for Biomedical Communications (LHNCBC) of the National Library of Medicine (NLM) is developing new tools and solutions that will facilitate patient-centric care, clinical research, and public health. These tools will solve the problem of tracking medication, needed preventive care, important laboratory tests and easily link to NLMs many rich resources of consumer-health databases. Specifically, this position will focus on research and development of open source

Job Advertised by HOSPITAL JOBS ONLINE- STAFF PHARMACIST JOB DESCRIPTION Description: The Staff Pharmacist position, provides pharmaceutical care services to the patients of the hospital including, but not limited to oversight, monitoring, preparation, dispensing and proper documentation of patient medication therapy as well as providing drug information, patient information and oversight of information and dispensing systems. The successful candidate will work with the team to ensure compliance with

Job Advertised by HOSPITAL JOBS ONLINE- A prominent, local area hospital is currently seeking a strong Clinical Pharmacist/Supervisor for its weekly day shift schedule. No weekends are associated with this position. They are eager for an individual with an excellent background in hospital pharmacy and a passion for patient care. Position Offers: --Extremely strong and honest management --Very clinically focused practice, carrying a terrific reputation --Team-oriented and customer service driven culture

Job Requirements An active State of Maryland pharmacy license...

Job Advertised by HOSPITAL JOBS ONLINE- A very financially stable facility is actively seeking a strong Clinical Pharmacist. This full-time, Monday-Friday, 9:30am-6pm position is a great opportunity for a pharmacist to receive quality experience in a Home Infusion setting. Occasional on-call weekends are a possibility. This pharmacist must be a team-leader who is looking to make a strong clincial impact and has a passion for patient care. Position Offers: --Strong leadership and management --Great

Responsible for all aspects of clinical study planning and execution within pre-specified program plans (resources, time lines, budgets, relationship management, identification of project risks & contingency plans); Provide overall cross-functional leadership to achieve project objectives on time, within budget and with high partnership satisfaction; Execution of clinical development program from protocol design collaboration to the final clinical study report for one to several studies; Coordinate all efforts

CRO in Greater DC Area has a permanent opening for a Clinical Project Manager. Responsibilities: Write protocols, investigational brochures, consent forms, clinical development plans, clinical study reports, clinical contracts and other related clinical documents for clinical trial research. Assist with the preparation of proposal requests for government funding, review safety data, and work as a team to prepare submissions to FDA/CBER. Coordination and supervision of clinical studies in accordance

Primary Purpose of this Position: The Clinical Program Manager is responsible for the planning, organization, and implementation of domestic and global clinical trials for cellular therapies and interacts with contractors, clinical investigators, and consultants to ensure compliance with FDA and international regulations, GCPs, and SOPs, and program data quality and efficiency Principal Responsibilities: Lead the selection and management of a Clinical Research Organization Lead regular Clinical Project

LICENSURE CERTIFICATION Current Maryland Registered Pharmacist license...

Job Summary: The Lead Clinical Pharmacist works under the supervision of the Pharmacy Manager, and/or Director of Pharmacy and is responsible for leading and developing systems and processes to ensure safe, appropriate, cost-effective medication therapies for patients according to established policies, procedures and protocols especially related to inpatient and outpatient Anticoagulation Management. They also coordinate clinical pharmacists and clinical activities of staff pharmacists in the area of anticoagulation

Job Summary: The Lead Clinical Pharmacist works under the supervision of the Pharmacy Manager, and/or Director of Pharmacy and is responsible for leading and developing systems and processes to ensure safe, appropriate, cost-effective medication therapies for patients according to established policies, procedures and protocols especially related to inpatient and outpatient Anticoagulation Management. They also coordinate clinical pharmacists and clinical activities of staff pharmacists in the area of

Kforce is currently seeking a Clinical Data Coordinator (CDC) for a position in Rockville, MD. The CDC will be responsible for assisting with the day-to-day data management tasks conducted for assigned projects. The CDC provides input into the development of Project Specific CRFs, departmental SOPs, and process improvements, and may participate the training of other CDCs. The incumbent will also participate in study set-up and lock, annotating CRFs, query management, and discrepancy management. Additionally

Current licensure by the Maryland State Board of Pharmacy is required 3...

Job Requirements An active State of Maryland pharmacy license B S or Pharm D...

Location Bowie Maryland Responsibilities Identify standards of care for cardiac...