Scientist, Pharmacology Cover Letter

Please consider me for the scientist, pharmacology opportunity. I am including my resume that lists my qualifications and experience.

Previously, I was responsible for sample analysis support to discovery teams focused on identifying biologics for the treatment of severe unmet medical needs in oncology, inflammation, autoimmunity and fibrosis.

Please consider my qualifications and experience:

• PhD in Pharmacokinetics, Pharmaceutical Sciences, Engineering, or related fields with equivalent professional degrees
• Expertise in PK/PD modeling and population-based analyses/simulations with established track-record records of model-based drug development
• Experience in supporting preclinical/clinical PK, PK/PD, and modeling & simulation components of regulatory documentations
• Excellent interpersonal, technical, and communication skills to lead cross-functional teams
• Demonstrated experience with modeling and simulation software
• Previous record of scientific contributions through peer-reviewed articles and external presentations
• Experience in clinical/nonclinical PK/PD study design, implementation and interpretation
• Extensive hands-on experience with non-compartmental and compartmental PK/PD analysis using WinNonlin software

Please consider me for the scientist, pharmacology opportunity. I am including my resume that lists my qualifications and experience.

In my previous role, I was responsible for scientific support to further development of established pharmaceuticals in the area of pharmacology and pharmacokinetic studies.

My experience is an excellent fit for the list of requirements in this job:

• Work closely with the Study Director to write or contribute to study protocols
• Plan and coordinate study logistics with study team
• Collaborate with supporting groups regarding study execution
• Conduct experiments according to study protocols in a safe manner and according to SOPs and GLP regulations
• Document results and accurately record observations in accordance with GLPs and SOPs
• Perform data analysis and maintain study records and effectively communicate study events with study participants
• Participate in summarizing data, data interpretation, including verification/QC review of study data, notebooks, and study reports
• May serve in the role of Contributing Scientist or Study Director on exploratory and/or GLP studies, with appropriate training and oversight

I am excited to be applying for the position of scientist, pharmacology. Please accept this letter and the attached resume as my interest in this position.

Previously, I was responsible for clinical expertise for identification and validation of novel targets, including the design of preclinical and/or clinical pharmacology experiments to validate targets and/or pathways.

My experience is an excellent fit for the list of requirements in this job:

• Experience with population PK/PD using appropriate software such as NONMEM/R/SPLUS in clinical drug development
• Experience with GLP procedures and documentation or equivalent familiarity with FDA guidance’s
• Experience with preparing clinical pharmacology/PK/PD related sections in regulatory submissions (i.e., IB, IND, NDA, MAA, BLA)
• Demonstrate a high level of initiative in troubleshooting experiments
• Fluent English written and spoken skills
• Demonstrable knowledge and experience in GPCR pharmacology and biology
• Knowledge and hands-on assay development experience with GPCR targets and cellular assays using radiometric, fluorescent and luminescent read-outs
• Proven track record in assay automation and high-throughput fluidics

Please consider me for the scientist, pharmacology opportunity. I am including my resume that lists my qualifications and experience.

In the previous role, I was responsible for oversight and work closely with collaborators and CROs in study protocol/report review for both preclinical and clinical studies.

Please consider my qualifications and experience:

• Experience working with cross-functional teams and serving as a point-of-contact for the team
• Strong organizational skills and able to work in compliance with the Novartis Code of Conduct and in accordance with Novartis guidelines on health and safety and data recording
• Hiring level will be commensurate with education and experience
• Experience with bioluminescent imaging, FACS, IHC, ELISA, RT-PCR, Westerns, or Luminex® is desirable
• Experience in writing technical drafts for IND (US-FDA) or CTA (EMA) filings is preferred
• A basic and or working knowledge of disease processes and mechanisms, available treatment paradigms, and patient populations within assigned Therapeutic Area is preferred.6716170330
• Familiarity with biochemistry/biophysics or molecular/cellular pharmacology with experience in assay development and biophysical methodologies supporting mechanism of action studies or hit/lead validation
• Knowledge of semi-automated liquid handling systems is desirable

I am excited to be applying for the position of scientist, pharmacology. Please accept this letter and the attached resume as my interest in this position.

Previously, I was responsible for scientific expertise, establish, and monitor external scientific collaborations, studies in CROs, monitor & provide critical assessment of competitor activities.

I reviewed the requirements of the job opening and I believe my candidacy is an excellent fit for this position. Some of the key requirements that I have extensive experience with include:

• PhD and postdoctoral experience in Biology, Pharmacology, or related field
• Industrial working experiences, especially the experiences in leading in vivo cancer pharmacology studies is preferred
• Solid hands-on skills in cell culture, cell/tumor implantation, drug administration and tissue sampling
• Extensive experience in developing, executing and implementing animal models independently
• Innovative mindset and strong collaborative spirit
• Keen interest and demonstrated experience in the field of anti-infective / chemotherapeutics
• Strong quantitative skills with hands-on experience in advanced data analyses, population PK, PK/PD, and exposure-response analyses
• Competent in the use of various modeling software (NONMEM, SAS, Splus, R, ) and standard noncompartmental data analysis software (Phoenix/WiNonlin)