Sourcing Associate in New Brunswick, NJ

 Job Description: Description:

Leads/supports execution of sourcing projects in collaboration with Procurement category owners and sourcing managers. Major responsibilities and accountabilities include:

• Support and/or lead execution of procurement plans depending on category/project complexity
• Assist with identification & screening/selection of potential sources and recommend appropriate sourcing method
• Assist with preparation of competitive go-to-market events (solicitation of bids, quotations and proposals) with pertinent specifications, terms and conditions.
• Evaluate proposals, assess risk and recommend overall best offer for a product or service
• Assist in the preparation of and/or issue contracts and SOWs (or large purchase orders) for legal review and approval
• Maintain agreement files as required
• As part of implementation, review product availability and/or pricing information with suppliers
• Provide internal and market analytics to support capture of best value for Client
• Prepare periodic category performance reports for assigned categories

Qualifications:

Requirements:
• Bachelor’s Degree in Finance, Supply Chain, Science, and/or Engineering
• 2-4 years of work experience
• 1-3 years Procurement/Procurement
• Prior work experience in Clinical Research, Drug Discovery, Product Development a plus
• Demonstrated ability to work in a fast-paced dynamic environment is required
• Strong analytical and communication skills (written and verbal)
Strong Contract management skills
• Proficiency in Ariba, Microsoft Word and Power Point and Excel (advanced)
• Proven ability to manage multiple projects/tasks effectively
Additional Job Requirements:
None
 
Note: Please allow me to reiterate that I chose to contact you either because your resume had been posted to one of the internet job sites to which we subscribe, or you had previously submitted your resume to Axelon.  I assumed that you are either looking for a new employment opportunity, or you are interested in investigating the current job market.

If you are not currently seeking employment, or if you would prefer I contact you at some later date, please indicate your date of availability so that I may honor your request. In any event, I respectfully recommend you continue to avail yourself to the employment options and job market information we provide with our e-mail notices.

Chandiran Murugan
Recruiter
Axelon Services Corporation
44 Wall Street 18th Floor
New York, NY 10005
Phone: (212) 384-6592
Fax  : (212) 306-0191
chandiran.murugan@axelon.com

Epidemiologist - Remote Contract Assignment -12 months

 Job Type: W-2 Contract

Duration: 12 months

Location: Boston, MA, full remote work preference for candidates from MA, CT, NY states

 

Job Overview

Our client is seeking an experienced Epidemiologist (Pharmaceutical) who will support the development, coordination, and execution of cutting-edge, effective, and impactful research for rare disease epidemiology at a global level, including deliverables to improve disease understanding supporting clinical development programs, regulatory submissions, and drug safety evaluations. 

 

·         Plan, support and execute analyses using the aHUS registry data and other hematology/nephrology indications, collaborating with internal staff and CROs.

·         Work closely with Senior-level Epidemiologists in the Department and may represent the Epidemiology department in cross-functional teams. 

·         Work with Epidemiology Department leadership to interface with key senior management and external stakeholders to ensure appropriate communication of results from epidemiology deliverables. 

·         Summarize results in written reports and oral presentations.

·         Support planning and execution of epidemiology deliverables relevant to drug development to characterize incidence and prevalence, time trends, co-morbidities, and co-medications.

·         Systematic identification and critical appraisal of epidemiological literature to characterize incidence, prevalence, natural history, and phenotype/genotype associations.

·         Oversee development of epidemiology sections of Regulatory, Pharmacovigilance, and Clinical Development documents, including Orphan Drug Applications, Risk Management Plans, PSURs/DSURs.

·         Participate in cross-functional team meetings with presentation of summary findings to internal/external stakeholders and support development of Epidemiology department processes and procedures.

 

Skills and Qualifications

·         Education: Master's Degree (MPH / MSc) in Epidemiology, Biostatistics, or relevant degrees

·         At least 3 years of industry experience in the pharmaceutical industry, biotechnology, or consulting environment

·         Knowledge of drug and clinical development process

·         The ideal candidate will have prior experience with analysis and interpretation of epidemiologic data within the context of rare disease and will be passionate about the application of epidemiology to support developing and delivering life-transforming therapies for patients.

·         Strong analytical skills in conducting analyses using registry or secondary data

·         Excellent oral and written communication skills

·         Excellent attention to detail and quality, and scientific rigor

·         Ability to work under pressure and lead by example

·         Strong interpersonal skills and ability to work effectively in multidisciplinary teams

·         Thorough and up-to-date technical knowledge of epidemiology and biostatistics methods

·         Must have mature team-working behaviors with organizational awareness and insight.  

 

Interested candidate should email john@... their resume, target rate and how they match the requirements.

Please visit our website at www.itechcp.com for more information about our company and a list of our hot jobs.

Best regards,

John Barry
ITech Consulting Partners

Recognized by Forbes as one of America’s Best Recruiting Firms in 2020 in the Professional Search Category

8 Wedgewood Court 
Newtown, CT 06470
203-270-0051 

john@itechcp.com

Committee Review Specialist – LMR, PromoMats – Contract– 100% Remote

 Job # : 21-00352

Job Title : Committee Review Specialist
Job Location : Tarrytown, NY 10591   *****REMOTE, 6 MONTHS
Travel Required : No
Overtime Required : No
Position Type : Contract
Job Description :

• Strong customer service ethic with demonstrated ability to interact with management, customers, vendors and partners.
• Experience executing operational processes within expected SLAs / timelines.
• Experience with compiling process metrics and identifying improvement opportunities.
• Outstanding communication skills, both written and verbal.
• Proactive, self-motivated, and able to work well in dynamic environment.
• Familiar with the drug development and commercialization process.
• Experience managing a Legal, Medical, Regulatory (LMR) review committee, preferred

​***send resumes

Arnise Frederick

SR. TALENT ACQUISITION SPECIALIST
__
 
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