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Requirements:
Pluses:
Refer to Job#13280-Sconsig and email MS Word attached resume to
Orly Miller
Email:
Requirements:
or
Pluses:
Refer to Job#13282-Sconsig and email MS Word attached resume to
Orly Miller
Email:
Requirements:
Refer to Job#13315-Sconsig and email MS Word attached resume to
Howard Fishman
Email:
Requirements:
Salary: $60-90k
BACKGROUND
Specifically, this person must:
At Adknowledge, we like to continually try new analytic approaches and use whatever works. We are not opposed to making large-scale changes if the cost/benefit is appropriate. This position will drive analytic changes with large implications for our company's bottom line.
QUALIFICATIONS
In addition to skill sets, this individual should:
This position will:
At Adknowledge, we like to continually try new analytic approaches and use whatever works. We are not opposed to making large-scale changes if the cost/benefit is appropriate. This position will drive analytic changes with large implications for our company's bottom line.
QUALIFICATIONS
In addition to skill sets, this individual should:
This position will be charged with:
QUALIFICATIONS
This is a long process, but we firmly believe that our employees are our most valuable assets. Successful applicants can be assured that they will work with the best and the brightest in our industry. Job is located at our headquarters in Kansas City, Missouri.
The successful candidate must be a visionary with the ability to conceive sophisticated and innovative solutions to real business problems and the desire to see them used in real world application.
JOB DESCRIPTION
QUALIFICATIONS
RECRUITMENT PROCESS
Multiple jobs listed for the states of WA, CA, MD and CT.
Click here to open this PDF document to see the details and contact information
Computer programming position working with clinical trials data. Provides programming support for creation and maintenance of programs used for data management; data validation; statistical report generation; and program validation. Assists Data Management and Biostatistics with developing tools and techniques for improving processes. Communicates effectively within a multi-disciplinary project team to complete assigned tasks on time and within budget.
Requires experience with SAS, SQL, PL/SQL, MS Access, Crystal Reports and large complex data systems. A strong understanding of Oracle databases and SAS datastep programming and report generation is also necessary. Candidates must demonstrate strong attention to detail with excellent problem solving and organization skills as well as the ability to effectively manage multiple assignments with challenging deadlines. Must have strong written and verbal communication skills; the ability to work as a member of a multi-disciplinary project team and a positive attitude and enthusiasm toward work. Prefer work experience in a research setting.
A diverse workforce enables us to achieve breakthrough advancements - an Equal Opportunity Employer.
Responsible for supervisory and management functions of the programming staff within Biostatistics, including hiring, training, mentoring and resourcing staff as well as tracking project timelines across Biostatistics for effectively hiring and resourcing staff on projects. Must effectively communicate priorities and work direction to complete assigned tasks on time and within budget and assist Biostatistics with developing tools and techniques for improving process efficiencies.
Requires a Bachelor's degree, preferably in Statistics, Computer Science, Biology or related field (MS desired). Five or more years of clinical research or related experience, including SAS programming and supervisory experience is also necessary.
A diverse workforce enables us to achieve breakthrough advancements - an Equal Opportunity Employer.
As the senior manager of Program Managers and Associate Directors, you will support Biostatistics and Data Management, coordinating the development/implementation of global SOPs. In this position, you will interact extensively with a multidisciplinary team, identifying critical needs and developing strategic initiatives. We’ll rely on you to improve processes and implement programming standards throughout the US and European sites to increase workflow efficiencies.
Requires a BS in Biology, Statistics, Computer Science or related field or equivalent experience and 9+ years of clinical research/management experience. (An MS is preferred.) Strong knowledge of FDA clinical trial guidelines and experience developing/managing staff are essential and working knowledge of clinical trial- related computer systems (Oracle Clinical, Clintrial, SAS, etc.) is desired. The ideal candidate will demonstrate initiative, leadership and show the ability to motivate others, leading multidisciplinary groups across several sites. You will participate in business development activities to acquire new business.
A diverse workforce enables us to achieve breakthrough advancements - an Equal Opportunity Employer.