Clinical Information Specialist Job - Memphis TN, 37501

Memphis Clinical Information Specialist Job - TN, 37501

alt-lib Suggests: Clinical Research Manager Job - Wilmington DE, 19801

MD not required for this one, so I'm suggesting it for anyone with healthcare/hospital/medical devicemaker/pharma background (and library experience, of course) : Wilmington Clinical Research Manager Job - DE, 19801

alt-lib Suggests: Copyeditor, Cell Press - Cambridge, MA - Elsevier

Copyeditor, Cell Press (click link to get to 'Apply Online' Button)
[EXCERPT FOLLOWS]

Copyeditor, Cell Press-SCI000FT

Elsevier : NA-United States-Massachusetts 

Description

 Cell Press, an imprint of Elsevier, currently seeks a copyeditor to work within our Cambridge-based production team. Our copyeditors edit scientific research articles prior to publication. Although scientific literacy is helpful, copyeditors are not expected to have a scientific background. Topics include genetics, molecular biology, cellular and developmental biology, neuroscience, and immunology. A large component of the work involves electronic editing of text for accuracy, mechanics, and journal style. 

Qualifications

 Our perfect candidate will pay close attention to detail, possess exceptional English language skills, and work well independently in a deadline-oriented environment. A degree in English/Journalism or life science is preferred, 1-2 years of related experience a plus. Computer literacy required. The preferred level of education for this position is a bachelors level degree.

....

 

Unposting Date

 Ongoing

alt-lib Suggests: Study Associate Job - Wilmington DE, 19801 - Yoh.com

Some of the elements of this job description, that makes me include it in my suggestions:

-Set-up, populate and accurately maintain information in tracking and communication tools (e.g. IMPACT, ISSIS, Clinical Partners Portal and eRoom*) and support others in the usage of these systems.
-Initiate and maintain production of study documents, ensuring template and version compliance.
- Provide input into non-drug project work including training activities and development of procedures as needed.
- Liaise with internal and external participants and/or vendors.
- Prepare, contribute to and distribute presentation materials for meetings, newsletters and web-sites.

* these are document management systems. - alt-lib

Original post: Wilmington Study Associate Job - DE, 19801

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Study Associate Job

Apply now »

Date: Jan 3, 2012

Location: Wilmington, DE, USA

Yoh has a contract opportunity for a Study Associate to join our client located in Wilmington, DE.

Job Overview:

Participate in the coordination of and contribute to operational activities to ensure quality and consistency of deliverables to time, cost, and quality objectives from Study Specifications (SS) through study close-out activities and Clinical Study Report (CSR).

Job Responsibilities:

- Contribute to clinical study start-up, execution, close-out and reporting. - Collect, review and track regulatory and other relevant documents. - Interface with Investigators, Strategic Partners, Marketing Companies and internal staff during the collection process to support effective delivery of a study and its regulatory documents through finalization of the Clinical Study Report (CSR). - Initiate and lead the set-up of the Study Master File (SMF) including tracking of documents. - Maintain and close the SMF ensuring International Conference of Harmonisation Guidelines for Good Clinical Practice (ICH/GCP) compliance. - Initiate and maintain production of study documents, ensuring template and version compliance. - Create and/or import clinical-regulatory documents into the Global Electronic Library (GEL) according to the Global Document List (GDL) ensuring compliance with the Authoring Guide for Regulatory Documents to support publishing in GEL. - Contribute to electronic applications/submissions by handling clinical-regulatory documents according to the requested technical standards (i.e. Submission Ready Standards (SRS), supporting effective publishing and delivery to regulatory authorities). - Plan and proactively collate the administrative appendices for the CSR. - Interface with Data Management Centre and/or Data Management Enablement representatives to facilitate the delivery of study related documents. - Provide input into non-drug project work including training activities and development of procedures as needed. - Set-up, populate and accurately maintain information in tracking and communication tools (e.g. IMPACT, ISSIS, Clinical Partners Portal and eRoom) and support others in the usage of these systems. - Manage and contribute to the coordination and tracking of study materials and equipment. - Coordinate administrative tasks during the study process, audits and regulatory inspections, according to company policies and SOPs. - Lead the practical arrangements and contribute to the preparation of internal and external meetings (e.g. study team meetings, ISS review meetings, monitor meetings, Investigator meetings, etc.). - Liaise with internal and external participants and/or vendors. - Prepare, contribute to and distribute presentation materials for meetings, newsletters and web-sites.

Job Qualifications:

- Minimum 1 year experience. - Level of education that supports skills and capabilities of the position and ensures successful conduct of accountabilities/responsibilities and appropriate interactions with internal/external customers. - Proven organizational and analytical skills. - Previous administrative training/experience. - Computer proficiency. - Excellent knowledge verbal, written and presentation communication skills. - Develop working knowledge of the Clinical Study Process and an understanding of the range of working procedures relating to it, together with an understanding of the ICH/GCP guidelines. - Ability to develop advanced computer skills to increase efficiency in day-to-day tasks. - Demonstrate ability to work independently, as well as in a team environment. - Ability to prioritize and manage multiple tasks with conflicting deadlines. - Good interpersonal skills and ability to work in a team environment. - Willingness to travel both domestically and internationally. - Proactively identify risks and possible solutions. - Demonstrate analytical thinking, concern for standards, concern for impact, good team skills including cooperation, willingness to learn from others, sharing relevant information, adaptability, self-control, tenacity conflict resolution skills and the ability to influence others. - Develop knowledge of therapy area through experience and review assignment.

....
Recruiter: Daniel Barrett


Yoh is a professional staffing provider with over 70 years of experience in the short- and long-term staffing services industry; visit our website to learn more about our company.


Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V.


J2W: SCIENTIFIC


MONJOB


J2WNWPHA

Ref: 978274

alt-lib Suggests: Grant Payment Analyst Job -Horsham PA, 19044- Yoh.com

Note: Many job postings that say MBA are applicable. What the recruiters are looking for is someone who has masters level education, in the adminstration  of business (ie, information) processes. -alt-lib

Horsham Grant Payment Analyst Job - PA, 19044

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Grant Payment Analyst Job

Apply now »

 

Date: Jan 9, 2012

Location: Horsham, PA, USA

Yoh has a contract opportunity for a Contract / Grant Payment Specialist to join our client in Horsham, PA.

Job Responsibilities:

Under the guidance of the manager, the incumbent will undertake the activities of the medical program financial specialist function within the operations group for a specified therapeutic area.

- The general focus of this Medical Program Financial Specialist group is to provide specialized support and assistance to Physicians and Medical Program Coordinators in the planning, execution and control of all global clinical grant financial administrative functions. - This function includes but is not limited to: budgets (planning, negotiating and administration), outsourcing, procurement and legal review to support clinical study programs. - This position encompasses complexities inherently involved with the efficient facilitation of global clinical grant financial administration as well as influencing the quality of information gathered, evaluated and reported in support of Medical Research Liaisons financial need.

Job Qualifications:

- Bachelor's degree in appropriate scientific or financial discipline. - Minimum of four years experience and/or equivalent competencies in pharmaceutical industry/clinical research or MBA/Master's degree plus two years experience in the pharmaceutical industry/clinical research. - This must include a working knowledge of the clinical development process with one to two years experience and/or equivalent competencies in financial administration

....

Recruiter: LaTanya Hill Yoh is a professional staffing provider with over 70 years of experience in the short- and long-term staffing services industry; visit our website to learn more about our company. Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/ J2W: CLINICAL MONJOB J2WMIDATL Ref: 978726