Supporting the medical writing team in the development of protocol design as well as CSR review and input. Interacting with Business Development for all proposal development support related to therapeutics for Oncology. Applicants must meet the following qualifications:
A software engineers and designers network is searching for a person to fill their position for a Telecommute Design Blog Editor. Core Responsibilities of this position include:
Design and timely complete all biological performance studies. Assist with product evaluation, efficacy and benefit demonstrations. Conduct biological trials in crops not readily available at other locations. Required Skills: Make presentations at scientific meetings.
Initiate, design, develop, execute and implement projects. Plan, conduct and prepare technical reports, data reports and other publications. Develop approaches for understanding, characterizing and organizing natural phenomena. Applicants must meet the following qualifications:
Providing direction and support to the Clinical Operations study team. Being the primary point of contact for Clinical Operations aspects of designated projects and responsible for developing successful working relationships with clients. Must meet the following requirements for consideration:
Engaging in the front end review and design of research trials for new and existing technology. Being the interface between the company and the genetic companies to design collaborative nutrition research. Writing papers and presenting the same at major technical and industry events.
Perform UAT testing on eDC study build. Design eCRFs within Medidata Rave. Must meet the following requirements for consideration: BS or MS in any stream. Must have at least 3 yrs. working in MediData Rave. Must have at least 8 years experience working as a data manager for clinical trials.
A nonprofit organization is filling a position for a Telecommute Research Associate. Core Responsibilities Include: Helping develop designs for experiments, define metrics, evaluate controlled and uncontrolled biases, and assess external validity of studies.
15 years of clinical design and operation experience in the pharmaceutical or biotechnology industry. Extensive experience with compliance issues and strong understanding of FDA regulations, GCP and/ SOPs in clinical research within a pharmaceutical or biotech environment.
Understand requirements and strategically implement robust software design. Researching and implementing the newest big data technologies to create solutions at scale. Qualifications for this position include: Willingness to travel to Colorado for at least 1 week a month.