 |
Sangamo BioSciences,
Inc. (Nasdaq: SGMO) is a biotechnology company
focused on the research, development and commercialization
of ZFPs for gene regulation
and gene modification.
Sangamo provides a friendly and casual work environment
that is intellectually inspiring and professionally
stimulating. Sangamo has excellent growth opportunities
for highly qualified and motivated individuals.
We offer competitive compensation and benefits; Health,
Dental, Vision and Life insurance, 401(k), Employee
Stock Purchase Plan, and a 125 cafeteria plan. Successful
candidates will have the opportunity to join a dyanamic
team and become a key player in the development of
a powerful technology into a novel therapeutics platform.
Job Openings
The following is a list of open positions with Sangamo BioSciences. (Updated 03/02/2010)
Clinical Research Associate III
Clinical Research Associate II
Scientific Programmer (Programmer / Analyst I)
Clinical Research Associate III
Essential functions include, but are not limited to the following:
Assist in the design, planning and implementation of clinical research projects
Manage the development of protocols, Investigator Brochures, case report forms, informed consents, study manuals and study budgets
Negotiate and finalize site contracts and budgets, manage and calculate site payments
Perform site visits including site qualification, initiation, monitoring and close-out visits; co-monitor with regional monitors and review monitoring reports
Ensure adherence to the protocol providing for accurate data collection, documenting drug accountability and compliance with federal regulations
Represent Sangamo BioSciences in a professional manner; establish and maintain good relationships with investigators and study site personnel
Maintain frequent site contact; prepare and track required documentation and manage study supplies at clinical sites
Oversee and track project progress at assigned sites (patient status, safety/adverse events, CRF completion, payments, study drug supply, regulatory documents).
Review data listings on an ongoing basis
Assist in planning Investigator Meetings
Assist in preparing interim study analyses, annual reports, and clinical study reports
Manage external vendors, develop study specifications, and finalize vendor contracts; vendors may include and are not limited to Contract Research Organizations (CROs), central laboratories, interactive voice response service for randomization (IVRS)
Requirements
4 to 5 years of Pharmaceutical industry experience including direct site management
BA/BS degree in nursing, pharmacy, life sciences or health-related discipline
Thorough knowledge of GCP, ICH and FDA regulations
Strong organizational skills, detail oriented, and able to multi-task and work effectively in a fast-paced environment
Self-motivated, assertive and able to function independently or as part of a team
Strong written and verbal communication; strong interpersonal skills.
Ability to travel 30-40%
back to top
Clinical Research Associate II
Essential functions include, but are not limited to the following:
Assist in the design, planning and implementation of clinical research projects
Assist in the development of protocols, Investigator Brochures, case report forms, informed consents, study manuals and study budgets
Facilitate the negotiation of site contracts and budgets, manage and calculate site payments
Perform site visits including site qualification, initiation, monitoring and close-out visits; co-monitor with regional monitors and review monitoring reports
>Ensure adherence to the protocol providing for accurate data collection, documenting drug accountability and compliance with federal regulations
Represent Sangamo BioSciences in a professional manner; establish and maintain good relationships with investigators and study site personnel
Maintain frequent site contact; prepare and track required documentation and manage study supplies at clinical sites
Oversee and track project progress at assigned sites (patient status, safety/adverse events, CRF completion, payments, study drug supply, regulatory documents).
Review data listings on an ongoing basis
Assist in planning Investigator Meetings
Assist in preparing interim study analyses, annual reports, and clinical study reports
Requirements
2 to 3 years of Pharmaceutical industry experience including direct site management
BA/BS degree in nursing, pharmacy, life sciences or health-related discipline
Thorough knowledge of GCP, ICH and FDA regulations
Strong organizational skills, detail oriented, and able to multi-task and work effectively in a fast-paced environment
Self-motivated, assertive and able to function independently or as part of a team
Strong written and verbal communication; strong interpersonal skills.
Ability to travel 30-40%
back to top
Scientific Programmer (Programmer / Analyst I)
Sangamo seeks a talented computer programmer (or scientist with exceptional programming skills) to fill an open position in our Technology group. The successful candidate will work with the group to improve our core protein design platform and related bioinformatics tools. Critical activities will include maintenance of our relational databases, data mining for patterns and trends, and the development of custom analysis scripts and web-based tools. The position requires adaptability, creativity and a capacity for constant innovation in pursuit of company goals. The work is exciting, fast-paced and directly impacts the company’s scope and capabilities.
Requirements:
B.S. in computer science, biology, chemistry or related field
Proficiency with python (or proficiency with PERL, JAVA or C/C+ and the ability to learn python)
A demonstrated proficiency in bioinformatics (i.e. a degree, a relevant scientific publication, or work experience)
Familiarity with UNIX-based operating systems
Strong written and oral communications skills
An ability to work in a team-oriented, multidisciplinary environment.
Additional attractive qualities include:
A graduate degree in computer science, biology, chemistry or related field
The ability to program in R or other statistical computer languages
Experience with relational databases
Experience with web-based applications.
If you feel you are qualified for this position, please send a cover letter and your resume / CV in electronic form to jobs@sangamo.com
.
back to top
Requirements are consistent with position levels and duties.
Salaries are commensurate with experience levels.
In addition to a competitive salary and excellent benefits, Sangamo offers stock options.
Sangamo is an equal opportunity employer.
|
|
|
