Kelly Services In Vivo Sr Research Associate in San Diego, California
In Vivo Research Associate II, San Diego, CA
As a Research Associate II / Sr. Research Associate, you will be be responsible for helping the company meet their goals in serving and maintaining clients and engaging in a number of projects in parallel, with multiple responsibilities in preclinical research. As a Sr. Research Associate you will be responsible for supporting studies assigned to the team by consistently executing procedures according to protocol and associated SOPs in GLP and non/GLP settings. Although timeliness is essential, it is imperative to understand the importance of maintaining and understanding accurate timelines, accurate supply levels and communicating to the Department Manager(s) to successfully execute all the duties and responsibilities of this evolving position.
Job Duties and Responsibilities:
Best practices and standard processes in daily work which support efficiencies, quality, safety, with a customer service focus.
Basic lab animal handling skills and general lab sanitation.
Provide proactive animal care support to alert the InVivo team of environmental or unexpected/adverse study-related observations directly impacting animal welfare.
Consistently completing assignments on time.
Demonstrate ability to seek out appropriate personnel resources to address non-routine questions.
Demonstrate ability to comply with all laboratory SOPs and GLP policies.
Accurate entry of data including lab IT systems and databases.
Maintain appropriate documentation as required by protocols and SOPs according to GLP practices.
Perform basic bio-methods such as handling (i.e restraint, ear notch, clinical observations, body weights, and so on. Dosing (i.e. PO, SC,IP, IV and more), Sample collection (i.e. blood and tissue, and more), basic necropsy.
Must be proficient with computers and software such as Microsoft Word, Excel, PowerPoint.
Good communication and presentation skills.
Good organizational and problem-solving skills.
Present and interpret study data in meetings, as well as in written documents and reports.
Contribute to and initiate scientific ideas in line with corporate and program goals.
Maintain close communication with the program leaders so as to adhere to program goals and time schedules.
Must be flexible and open to new tasks and challenges
May administer treatments or mediations according to the orders.
Assist in general record-keeping as well as specialized monitoring and surveillance programs.
Observe and report changes in the health status or condition of animals.
May perform technical procedures.
May euthanize animals in accordance with procedures as directed by InVivo Supervisor/Manager.
Dispose of dead animals as outlined by standard operating procedures.
May collect blood samples and feces, urine, or other types of specimens from animals.
Performs other duties as assigned by management.
Assist in keeping facility neat and free of litter (may sweep, mop, dust, etc.).
Commitment to follow through on tasks and deadlines with minimal supervision in a safe manner.
Must be willing and able to work among and across most animal species.
A plus to understand and be able to develop and utilize in-vivo animal models.
A plus to understand and be able to compile data, prepare ACUP's, protocols, reports, prepare graphs, and analysis; GLP and non-GLP data documentation.
Able to work with and/or train to staff to work with bio-hazardous or radioactive materials.
Must possess a strong sense of urgency; occasional weekends, early mornings or late nights work may be required
Able to understand the internal and external needs and impact of duties and responsibilities.
Must be a flexible, self-starting and self-managing person.
Quick turn-around requirements on requests and accuracy and thoroughness is critical.
Ability to maintain confidential information in a professional manner.
Constantly observes condition of the property's interior and exterior and immediately reports and/or initiates actions to correct unsafe and/or unacceptable established conditions.
Travels between facilities, and at times to client locations.
Equipment / Tools / Skills:
An employee in this position must be knowledgeable and skilled in the safe use and maintenance of the following equipment and tools: Knows to use protective devices: gloves, goggles, mask, non-skid water safe shoes, etc.; Maintains awareness of proper safety precautions at all times; Always uses products and/or machines as recommended by the manufacturer's safety instructions.
Bachelor's degree (BS) in an appropriate biological discipline leading to a college level understanding of mammalian physiology, such as: Biology, Biological Sciences, Biochemistry, Physiology, or Pharmaceutical Sciences, Physiology / Pharmacology related in vivo laboratory environment.
Minimum three (3) years of In Vivo experience.
Knowledge of Vivarium and/or InVivo procedures and processes, preclinical study implementation and conduct.
Working knowledge of the process of conduction of non-clinical discovery and development studies in all relevant laboratory animal species.
Familiar with Drug Development Process and regulatory and clinical considerations.
Knowledge of Good Laboratory Practice regulations and ICH guidelines.
Understanding of USDA animal welfare regulations and AALAC guidelines is essential.
Additional experience working with cancer / diabetes / inflammation model highly desirable.
Positive approach and willingness to accept new projects as required.
Consistently seeks out self-improvement opportunities in all aspects with the purpose of improving and training self.
Sound reasoning ability to effectively prioritize and communicate.
Able to multi-task and execute with precise attention to detail.
Must have the ability to solve problems, offer solutions, think logically and have a quick and retentive memory.
Must be able to take direction however must successful work independently.
Must have strong organizational and analytical skills.
Ability to handle multiple tasks, respond quickly and efficiently, and keep situations under control, in a fast paced dynamic work environment.
Good record keeping and attention to detail essential.
Must be proficient with computers and software such as Microsoft Word and Excel.
Excellent communication skills are a must; Good organizational and problem-solving skills
Why Kelly ® ?
With Kelly, you’ll have access to some of the world’s highest-regarded scientific organizations—providing you with opportunities to work on today’s most challenging, research-intensive, and relevant projects. Our connections can lead you to innovative scientific pursuits you’ll be proud to help advance. We work with 95 of the Fortune 100™ companies, and found opportunities for more than 11,000 scientific professionals last year.
You pursued a career in science to fuel your quest for knowledge and your desire to make the world a better place. Let Kelly fuel your career—connect with us today.
AboutKelly Services ®
As a workforce advocate for over 70 years, we are proud to directly employ nearly 500,000 people around the world and have a role in connecting thousands more with work through our global network of talent suppliers and partners. Revenue in 2016 was $5.3 billion. Visit kellyservices.com and connect with us on Facebook , LinkedIn and Twitter .
Kelly Services is an equal opportunity employer including, but not limited to, Minorities, Females, Individuals with Disabilities, Protected Veterans, Sexual Orientation, Gender Identity and is committed to employing a diverse workforce. Equal Employment Opportunity is The Law. at https://www.dol.gov/ofccp/regs/compliance/posters/ofccpost.htm