Clinical Jobs in Delaware
Yoh has a contract opportunity for a Clinical Submissions Specialist to join our client in Wilmington, DE. Job Responsibilities: - Effectively communicate submission format requirements to the submission team. - Publish Clinical deliverables such as protocols and Clinical Study Reports - Collect necessary information and requirements from the submission team. - Compile and publish regulatory submi...
CLINICAL STUDY OPERATIONS SPECIALIST REQUIREMENT #13-00564 RECRUITER: CINDI PISNOY JOB LOCATION: WILMINGTON, DE JUNE 13, 2013 * CANDIDATE MUST WORK ON OUR W-2 ONLY* Project Description: Candidate will work with, and lead, cross functionality with internal and external partners on global studies across different phases of drug development and different therapy areas. Coordinate all aspects of study...
Yoh has an opportunity for a Clinical Research Associate for our client in Wilmington, DE. Job Responsibilities: - Leads the delivery of committed components for clinical studies according to agreed resources, budget and timelines complying with Procedural Documents, international guidelines such as ICH-GCP, as well as relevant local regulations. - Ensures that sites are identified, site qualifica...
Yoh has a contract opportunity for a Clinical Submissions Specialist to join our client in Wilmington, DE. Job Responsibilities: - Effectively communicate submission format requirements to the submission team. - Collect necessary information and requirements from the submission team. - Compile and publish regulatory submissions in accordance with current standards and processes using agreed upon t...
Clinical Research Associate w/PM Experience Keystone Computer Associates is a Minority-owned Business Enterprise (MBE) and a leading vendor for IT, professional and pharmaceutical staffing and recruiting services. Keystone has been in business since 1965 and is headquarted in Fort Washington, PA. We are currently searching for a high-level, in-house Clinical Research Associate with Project Managem...
Minimum Requirements • University Degree or equivalent • A specialist knowledge of contract and procurement management, with specific reference to the pharmaceutical/health care industry. • A demonstrated knowledge of contracting/commercial processes preferably from the CRO industry • A good understanding of procurement and project management tools and processes. • Comprehensive knowledge of clini...
About the Organization: EEO/Drug-Free Employer Description: HCR ManorCare provides a range of services, including skilled nursing care, assisted living, post-acute medical and rehabilitation care, hospice care, home health care and rehabilitation therapy. The Director of Nursing is responsible for the overall clinical operation of the hospice agency. Key responsibilities involve budgetary, managem...
DESCRIPTION: External Summary of Primary Responsibilities: MAJOR RESPONSIBILITIES: * Responsible for selling, maintaining and documenting all sales activities for the AstraZeneca CNS portfolio of products to physicians in community mental health facilities as well as office-based practices, private practice, in group practices, in hospital settings, and CNS residency and fellowship programs within...
Company: Siemens Medical Solutions USA, Inc. Division: SMSD - Diagnostics Location: DE - Newark Req ID: 122347 Position Title: Senior Director of Technical Operations (Consumables Manufacturing) Experience Level: Senior Level Education Required: Masters Degree or equivalent experience Travel Required: Yes Company Description: Siemens’ Healthcare Sector is one of the world's largest suppliers to th...
DESCRIPTION: External Summary of Primary Responsibilities: Responsibilities: - Function independently with a high degree of sales proficiency. - Develop superior product and disease state knowledge and effectively educate and engage healthcare professionals in dialogue about clinical evidence, approved indications, and product efficacy/safety profiles to support on-label prescribing for appropriat...
ASSOCIATE MEDICAL DIRECTOR, MD REQUIREMENT #13-00496 RECRUITER: KAREN GULUTZ JOB LOCATION: WILMINGTON, DE MAY 30, 2013 * CANDIDATE MUST WORK ON OUR W-2 ONLY * Minimum Requirements, Education, and Experience: · Medical degree · At least 2 years of clinical experience post-registration/certification · Proven medical competence, with an ability to balance this with industry standards to achieve busin...
Description The Senior Medical Information Manager is responsible for the execution of Medical Information-related brand/area deliverables including scientific review of promotional materials, creation and review of scientific materials for Medical Affairs and Strategic Development, and the creation and review of documents to address health care professional and managed market scientific questions...
DESCRIPTION: The Associate Director Medical Affairs (ADMA) is responsible for supporting the Director Medical Affairs (DMA) by leading the scientific content development and training for Medical Affairs activities in support of medical brand plan objectives. The ADMA works with the DMA to coordinate Medical Affairs services in support of the brand, and facilitating Field Medical brand activities....
This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. As a SSUA you will be responsible for the independent preparation, review and approval of country related submission packages in accordance with ICH, GCP and all applicable regulations, law...
Please send resume to email@example.com Our client has been around for more than 165 years, today they are active in around 190 regions, occupying leading market and technology positions worldwide with its business activities in the Energy, Healthcare, Industry, and Infrastructure & Cities Sectors. Overall, with 370,000 employees (continuing operations) around the world. Our client has partnered w...
Yoh has a contract opportunity for a Senior Clinical Study Operations Specialist to join our client in Wilmington, DE. Job Responsibilities: - Lead and manage large dynamic US investigator sponsored study programs. - Manage stakeholder relations; study budgets and project manage study. - Coordinate operational aspects Investigator Sponsored studies from SDC / Proposal through CSR / Publication. -...
This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. As an SSUA you will be responsible for supporting the Study Start Up Group by reviewing and negotiating Investigator contracts, budgets and related documents, ensuring timely completion and...
Description: Improve Your Quality of Life While Helping Seniors! Evercare is now part of the OptumHealth division under the greater UnitedHealth Group. As an OptumHealth Nurse Practitioner (NP) you will provide primary care to your caseload of patients in long term care settings. This excellent opportunity affords a flexible autonomous role bringing enormous satisfaction in the care and comfort of...
As part of Walgreens Health and Wellness division , Take Care Health Systems includes Take Care Consumer Solutions (www.takecarehealth.com), managers of convenient care clinics located at select Walgreens drugstores nationwide, and Take Care Employer Solutions (www.takecareemployersolutions.com), managers of worksite-based health and wellness services. The company combines best practices in health...
Yoh has a contract opportunity for an Associate Medical Director to join our client in Wilmington, DE. Job Responsibilities: - Start out reviewing and assessing individual Adverse Event reports, progressing to analyzing adverse event reports in the aggregate, which would lead to contributing to periodic reports (DSURs, PSURs, etc.) and ad hoc reports. - Assist in providing medical expertise and ju...
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Clinical Coordinator-Clinical Trials
$31,200.00 - $87,400.00
Typical Salary for Clinical Coordinator-Clinical Trials in Delaware
Source: Monster.com Careerbenchmarking Tool
Education / Training
Some College Coursework Completed
Source: Monster.com Careerbenchmarking Tool
Clinical Coordinator-Clinical Trials
Plans and controls clinical pharmacology studies by developing and implementing research and administrative strategies, exclusive of those actions requiring medical judgments; standardizing operating procedures across all trials; supervising staff.
Rate of Growth
Size of Industry in 2006:
Source: Bureau of Labor Statistics, May 2006
Administrative Writing Skills
Health Promotion and Maintenance
Improves quality results by studying, evaluating, and re-designing processes; contributing to the ongoing analysis and modification of protocols; preparing and recommending amendments to clinical trials protocols in conjunction with appropriate committees; implementing changes.
Meeting clinical trials financial standards by providing annual budget information; monitoring expenditures; identifying variances; implementing corrective actions.
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