Careers

Careers at Arvinas

Open Positions

Arvinas, Inc. is seeking qualified candidates for the following open positions:

Research Scientist/Senior Research Scientist (Androgen Receptor/Prostate Cancer)

Arvinas is a pharmaceutical company focused on developing new small molecules ‒ known as PROTACs (PROteolysis TArgeting Chimeras) ‒ aimed at degrading disease-causing cellular proteins via proteolysis. Based on innovative research conducted at Yale University by Dr. Craig Crews, Founder and Chief Scientific Advisor, the company is translating natural protein degradation approaches into novel drugs for the treatment of cancer and other diseases. The proprietary PROTAC-based drug paradigm induces protein degradation, rather than protein inhibition, using the ubiquitin proteasome system and offers the advantage of potentially targeting “undruggable” as well as “druggable” elements of the proteome. This greatly expands the ability to create drugs for many new, previously unapproachable targets.

Arvinas is seeking an innovative and collaborative biologist with expertise in prostate cancer biology. The candidate should be knowledgeable about the Androgen Receptor (AR) biology and experimental techniques employed to study nuclear hormone receptor signaling. The responsibilities involve conducting mode of action studies with existing and novel AR PROTACs. The ability to conduct and oversee in vivo prostate cancer model development is recommended.

EDUCATION AND TRAINING

Ph.D, with 0-3 years of post-doctoral experience in cellular and molecular biology, pharmacology or biochemistry. Previous experience in prostate cancer research is required.

RESPONSIBILITIES INCLUDE:

  • Culture and maintenance of cell lines, including generation of stable cell lines
  • Assessment of compound efficacy via biochemical and molecular biology techniques, such as immunostaining and immunoblotting (e.g. high content imaging, western, qPCR, reporter assay)
  • Interaction and collaboration with biology and chemistry team members to contribute to structure-activity relationship (SAR) determination
  • Solving methodological problems in experimental protocols and results
  • Documentation, compilation, analysis and interpretation of experimental data
  • Presentation of data in oral and written reports in a clear and concise manner to supervisor and project teams
  • Management of laboratory notebook, databases and/or spreadsheets to compile and present results in a meaningful manner
  • Staying up-to-date on relevant scientific literature

REQUIREMENTS

  • Innovative, motivated, researcher with strong problem solving and communication skills
  • Expertise in cell-based assays to study nuclear hormone receptor signaling
  • Demonstrated subject matter expertise via publications and/or external presentations

PREFERRED BUT NON-ESSENTIAL REQUIREMENTS:

  • Experience in developing novel assays and animal models in prostate cancer
  • Demonstrated success in working on a cross-disciplinary, drug discovery project team; integrating and evaluating the work of multiple drug discovery groups / functions
  • Expertise in developing compound profiling assays to support chemistry efforts in developing structure-activity relationships that guide lead identification, optimization & development candidate selection
  • Solid understanding of how to leverage biomarkers and translational research to guide development of personalized medicine
  • Knowledge of assays & metrics that report on potency, selectivity, ADME, PK, PD & efficacy

Location: New Haven, CT

Please send CV and cover letter to: careers@arvinas.com. Please denote in the subject line the specific position: AR/Prostate Cancer

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Head of Preclinical Sciences

The Head of Preclinical Sciences is responsible for overseeing the drug metabolism, pharmacokinetics and toxicology support for development candidate nomination and IND filings. Qualified candidates will be creative and detail-oriented with a passion for drug discovery, possess excellent project management, time management, communication, data analysis, and interpersonal skills, along with an overall understanding of, and direct hands on experience, in early-stage development within the biotech/biopharma industry.  This position will report to the Vice President, Biology.

Activities include, but are not limited to:

  • Collaborate with research project leaders to develop project-specific strategies to generate appropriate data to support development candidate nomination and IND filing
  • Oversee the design and management of pre-clinical studies (GLP and non-GLP) for inclusion in IND submissions, including ADME/PK and biodistribution and toxicology
  • Oversee the selection and management of consultants and contract research organizations (CROs) to support pre-clinical development programs
  • Manage projects conducted by CROs with efficient governance including contract execution, authorization of study amendments, schedule and budget variance management, progress reporting to stakeholders, review of data and draft study reports, completion of contract milestones, study close-out and alignment of preclinical development efforts with corporate drug development efforts and priorities
  • Write and edit pre-clinical study reports
  • Oversee drafting of the relevant sections and individual reports to support regulatory filing including pre-IND, IND, IB, and clinical lab manuals
  • Participate in discussions with FDA to obtain feedback on pre-clinical development programs
  • Contribute to clinical development plans
  • Ensure compliance with global pre-clinical studies regulatory guidelines

 

Basic Qualifications:

  • PhD or DVM and post-doctoral experience in Pharmacology, Drug Metabolism, Toxicology or Pathology and knowledge of biochemistry, cell biology, systems biology, and physiology.
  • Solid understanding of the drug discovery and development process based on at least 7-10 years of relevant experience in the biotech/pharmaceutical industry
  • Demonstrable contributions to regulatory filings and working knowledge of GLP, GCP and ICH regulations
  • Experience with the design and execution of in vitro/in vivo experiments to determine the effects of therapeutics on biological systems, with line of sight to human safety risk understanding.
  • Hands-on experience with in vitro toxicology, pharmacology and/or molecular biology experimentation to investigate molecular mechanisms of drug action.
  • Strong leadership competencies and management experience, including selecting CROs and overseeing the relationship.
  • Excellent written and oral communication, presentation and influencing skills Highly motivated, creative, innovative, reliable scientist, with a flexible, collaborative, team-oriented mindset, who solves problems in a goal-focused fashion and can excel in a fast-paced small company environment
  • A social personality that contributes to an open, positive, collaborative working climate.

 

Preferred Qualifications:

  • DABT certification and experience as GLP Study Director is preferred, but not required.
  • Working knowledge of human dose modeling

Location

New Haven, CT

Please send CV and cover letter to: careers@arvinas.com.

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Associate Director, Project Management R&D

Arvinas is a pharmaceutical company focused on developing new small molecules ‒ known as PROTACs (PROteolysis TArgeting Chimeras) ‒ aimed at degrading disease-causing cellular proteins via proteolysis. Based on innovative research conducted at Yale University by Dr. Craig Crews, Founder and Chief Scientific Advisor, the company is translating natural protein degradation approaches into novel drugs for the treatment of cancer and other diseases. The proprietary PROTAC-based drug paradigm induces protein degradation, rather than protein inhibition, using the ubiquitin proteasome system and offers the advantage of potentially targeting “undruggable” as well as “druggable” elements of the proteome. This greatly expands the ability to create drugs for many new, previously unapproachable targets. 

Key Responsibilities:

  • In partnership with team, drive and contribute to asset development team ensuring strategy and execution alignment
  • Develop, maintenance, proactive tracking and management of a high quality integrated project plans for multiple development projects
  • Facilitate discussions to drive towards program or initiative decisions
  • Identify, communicate and manage project and asset risks
  • Ability to conduct process analysis and develop and implement plans
  • Coordinate project team meeting and generate meeting minutes
  • Act as an interface with scientists to ensure smooth communication in internal programs as well as with external collaborators
  • Assists the development team responsible in the planning, implementation, and compliance of multiple aspects of Arvinas clinical trials using multiple vendors.
  • Willing to identify, development and/or implement forward thinking research and development initiatives to support company transformation

Qualifications:

  • Bachelor’s degree in Life Sciences or Pharmacy.
  • 8+ years in the pharmaceutical industry in roles associated with drug development
  • 5+ years supporting cross-functional drug development teams in core function
  • Must be able to work independently and collaboratively in a fast-paced, matrixed, team environment consisting of internal and external team members.
  • Superior communication and interpersonal skills; effective interaction with cross functional team members.
  • Experienced in managing multiple initiatives while working in a fast paced and dynamic environment.
  • Demonstrated planning, organization and time management skills including the ability to support and prioritize multiple projects.
  • Excellent problem-solving skills and the ability to adapt to changing priorities and deadlines.
  • Skilled in managing multi-disciplinary teams both internally and externally
  • Flexibility in understand the needs of teams.
  • Proficiency with Project Management related and Microsoft Office Software Programs.
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Computational Design Chemist

Arvinas is a pharmaceutical company focused on developing new small molecules ‒ known as PROTACs (PROteolysis TArgeting Chimeras) ‒ aimed at degrading disease-causing cellular proteins via proteolysis. Based on innovative research conducted at Yale University by Dr. Craig Crews, Founder and Chief Scientific Advisor, the company is translating natural protein degradation approaches into novel drugs for the treatment of cancer and other diseases. The proprietary PROTAC-based drug paradigm induces protein degradation, rather than protein inhibition, using the ubiquitin proteasome system and offers the advantage of potentially targeting “undruggable” as well as “druggable” elements of the proteome. This greatly expands the ability to create drugs for many new, previously unapproachable targets.

Arvinas, the industry leader in protein degradation science is currently expanding its computational chemistry group with an additional hire to support the design and optimization of PROTACs, bifunctional, chimeric molecules that recruit target proteins to E3 ligases for ubiquitination and degradation by the cells natural and selective protein homeostasis system.

POSITION QUALIFICATIONS

The successful candidate should be an industry-experienced computational chemist with postdoctoral experience in molecular dynamics simulation, free energy perturbation calculation and/or conventional docking, and an understanding of basic medicinal chemistry.

Experience in protein modeling or protein-protein interaction modeling is a strong plus, and an ability in scripting, computer networking or cloud instance management is desirable.

An ability to effectively prioritize and deliver on tight timelines, plus good oral and written communications skills are a must.

Experience in using computers and databases for data collection, compilation, analysis, and information dissemination is also required, as is proficiency with MS Word, PowerPoint, and Excel.

 

LOCATION

New Haven, CT.

Suitably qualified candidates should send their resume plus a cover letter to careers@arvinas.com.

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Platform Biology, Leader

Arvinas is a pharmaceutical company focused on developing new small molecules ‒ known as PROTACs (PROteolysis TArgeting Chimeras) ‒ aimed at degrading disease-causing cellular proteins via proteolysis. Based on innovative research conducted at Yale University by Dr. Craig Crews, Founder and Chief Scientific Advisor, the company is translating natural protein degradation approaches into novel drugs for the treatment of cancer and other diseases. The proprietary PROTAC-based drug paradigm induces protein degradation, rather than protein inhibition, using the ubiquitin proteasome system and offers the advantage of potentially targeting “undruggable” as well as “druggable” elements of the proteome. This greatly expands the ability to create drugs for many new, previously unapproachable targets. 

PhD-level position dedicated to conducting experiments to further understand the underlying principles of PROTAC-mediated protein degradation.

 

Education and Training

  • Ph.D, with 5+ years of pharma- or biotech experience in cellular and molecular biology, pharmacology, biochemistry, biophysics or enzymology. Focus on cancer cell biology and drug discovery strongly preferred.

Requirements

  • Innovative, creative, inquisitive, motivated researcher with strong problem-solving skills and demonstrated ability to advance new scientific understanding
  • Experience in the ubiquitin-proteasome system, or targeted protein degradation, preferred
  • Strong expertise in cancer cell biology, drug discovery approaches and biochemical and biophysical techniques
  • Strength in running and evaluating experiments to measure target engagement, protein degradation, pathway modulation and therapeutic sensitivity in response to compounds
  • Experience in developing assays to profile compounds using mechanistic and functional readouts
  • Demonstrated success in working on a cross-disciplinary, drug discovery project team; integrating and evaluating the work of multiple drug discovery groups / functions
  • Expertise in developing compound profiling assays to support chemistry efforts in developing structure-activity relationships
  • Excellent communication and interpersonal skills
  • Supervisory experience

Other Preferred Skills and Knowledge

  • Manages times and balances work between bench and desk
  • Maintains accountability for ensuring own goals, those of any direct reports and company objectives are achieved
  • Maintains a safe working environment for self and others
  • Represents the company effectively to external organizations and to the Board of Directors and other company senior management, as needed/requested
  • Writes procedures/protocols and professional/technical reports and writes scientific articles, publications and patents

Location

New Haven, CT

Please send CV and cover letter to: careers@arvinas.com.

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Associate Scientist / Sr. Associate Scientist (Biology) (4)

Arvinas is a pharmaceutical company focused on developing new small molecules ‒ known as PROTACs (PROteolysis TArgeting Chimeras) ‒ aimed at degrading disease-causing cellular proteins via proteolysis. Based on innovative research conducted at Yale University by Dr. Craig Crews, Founder and Chief Scientific Advisor, the company is translating natural protein degradation approaches into novel drugs for the treatment of cancer and other diseases. The proprietary PROTAC-based drug paradigm induces protein degradation, rather than protein inhibition, using the ubiquitin proteasome system and offers the advantage of potentially targeting “undruggable” as well as “druggable” elements of the proteome. This greatly expands the ability to create drugs for many new, previously unapproachable targets. 

Education and Training

  • BS/MS with 8+ years of Pharma/Biotech drug discovery experience

Preferred Skills and Abilities

  • Innovative, independent, motivated and productive problem solver with excellent communication skills who also works effectively in a team setting
  • Strength in experimental design, execution, and data analysis
  • Organized, goal-oriented and timeline-conscious
  • Strength in leveraging multiple assay platforms for measuring target engagement, pathway modulation and cell sensitivity in response to compounds or target modulation
  • Experience in design, QC and execution of medium- to high- throughput 96/384 well assay formats, such as ELISA, quantitative Western, cell viability/death
  • Molecular techniques: cloning, PCR, RT-PCR, cell line engineering
  • Protein expression and purification

Experience in utilizing compounds and molecular target manipulation (e.g. RNAi) to dissect target function and dependency

Location

New Haven, CT

Please send CV and cover letter to: careers@arvinas.com.

 

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Director/Senior Director, Project Leader, Biology

Arvinas is a pharmaceutical company focused on developing new small molecules ‒ known as PROTACs (PROteolysis TArgeting Chimeras) ‒ aimed at degrading disease-causing cellular proteins via proteolysis. Based on innovative research conducted at Yale University by Dr. Craig Crews, Founder and Chief Scientific Advisor, the company is translating natural protein degradation approaches into novel drugs for the treatment of cancer and other diseases. The proprietary PROTAC-based drug paradigm induces protein degradation, rather than protein inhibition, using the ubiquitin proteasome system and offers the advantage of potentially targeting “undruggable” as well as “druggable” elements of the proteome. This greatly expands the ability to create drugs for many new, previously unapproachable targets. 

Reports to: Vice President, Biology

 

Education and Training

  • PhD, with 15+ years of pharma or biotech drug discovery experience, preferably in oncology. Track record of leading research projects to IND-track nomination.

Position Summary

Responsible for the effective management of assigned therapeutic projects in line with company criteria and timelines within a matrix team environment, particularly in collaboration with partner Chemistry project lead

Provide transparent, focused updates to manager and company executives as requested and represent company at scientific conferences, regulatory body meetings and other external organizations as needed

May supervise/mentor junior PhD biologists

 

Requirements

  • Demonstrated success in leading a cross-disciplinary, drug discovery project team; integrating and evaluating the work of multiple drug discovery groups / functions
  • Innovative, motivated, researcher with strong problem solving and communication skills
  • Strong background in cancer biology and signaling with demonstrated expertise in incorporating this knowledge into drug discovery
  • Expertise in developing compound profiling mechanistic and functional assays to support chemistry efforts in developing structure-activity relationships that guide lead identification, optimization & development candidate selection, specifically, running and evaluating experiments to measure target engagement, pathway modulation and therapeutic sensitivity in response to compounds or target modulation
  • Knowledge of assays & metrics that report on potency, selectivity, ADME, PK, PD, safety & efficacy
  • Some bench work may be expected
  • Solid understanding of how to leverage biomarkers and translational research to guide clinical development
  • Contribute to regulatory documents, scientific publications, patents
  • Make scientific contributions that have significant impact on the Arvinas platform and overall research direction of the company
  • Maintain orderly and timely record of project plans and results in accordance with company policy and legal requirements
  • Accountability for ensuring own goals, those of any direct reports, project team goals, and project and company objectives are achieved
  • Excellent publication record
  • Maintain a safe working environment for self and others

Location

New Haven, CT

Please send CV and cover letter to: careers@arvinas.com.

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Research Scientist/Sr. Research Scientist (Biology) (1)

Arvinas is a pharmaceutical company focused on developing new small molecules ‒ known as PROTACs (PROteolysis TArgeting Chimeras) ‒ aimed at degrading disease-causing cellular proteins via proteolysis. Based on innovative research conducted at Yale University by Dr. Craig Crews, Founder and Chief Scientific Advisor, the company is translating natural protein degradation approaches into novel drugs for the treatment of cancer and other diseases. The proprietary PROTAC-based drug paradigm induces protein degradation, rather than protein inhibition, using the ubiquitin proteasome system and offers the advantage of potentially targeting “undruggable” as well as “druggable” elements of the proteome. This greatly expands the ability to create drugs for many new, previously unapproachable targets. 

Education and Training

  • Ph.D, with 3+ years of post-doctoral experience in cellular and molecular biology, pharmacology or enzymology. Focus on cancer cell biology and drug discovery preferred but not essential

Requirements

  • Innovative, motivated, researcher with strong problem solving and communication skills
  • Strong expertise in drug discovery approaches and scientific techniques
  • Strength in running and evaluating experiments to measure target engagement, pathway modulation and therapeutic sensitivity in response to compounds or target modulation

Preferred but Non-essential Requirements:

  • A Ph.D. or equivalent in biomedical research and a productive post-doctoral fellowship (at least 3 years) with a strong background in cancer biology and signaling and outstanding publications
  • Molecular-genetic understanding of cancer; facility incorporating this knowledge into drug discovery
  • Experience in developing assays to profile compounds using mechanistic and functional readouts
  • A demonstrated ability to be innovating and to advance new scientific understanding
  • Demonstrated success in working on a cross-disciplinary, drug discovery project team; integrating and evaluating the work of multiple drug discovery groups / functions
  • Expertise in developing compound profiling assays to support chemistry efforts in developing structure-activity relationships that guide lead identification, optimization & development candidate selection
  • Solid understanding of how to leverage biomarkers and translational research to guide development of personal medicine
  • Knowledge of assays & metrics that report on potency, selectivity, ADME, PK, PD & efficacy

Location

New Haven, CT

Please send CV and cover letter to: careers@arvinas.com.

 

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Sr. Associate Scientist/Research Scientist (Neurobiology)

Arvinas is a pharmaceutical company focused on developing new small molecules ‒ known as PROTACs (PROteolysis TArgeting Chimeras) ‒ aimed at degrading disease-causing cellular proteins via proteolysis. Based on innovative research conducted at Yale University by Dr. Craig Crews, Founder and Chief Scientific Advisor, the company is translating natural protein degradation approaches into novel drugs for the treatment of cancer and other diseases. The proprietary PROTAC-based drug paradigm induces protein degradation, rather than protein inhibition, using the ubiquitin proteasome system and offers the advantage of potentially targeting “undruggable” as well as “druggable” elements of the proteome. This greatly expands the ability to create drugs for many new, previously unapproachable targets. 

Arvinas is seeking a talented, innovative, and experienced biologist to investigate how targeted-protein degradation can impact neurodegenerative diseases. Successful candidates should be highly motivated and enjoy working in a team-based environment.

This position is laboratory-based and requires strong experimental skills with a background in cell biology, particularly with primary neuronal cultures, and experience in quantitative assay development, cell-based compound screening, biochemical assays, immunocytochemistry, and high-content imaging.

EDUCATION AND TRAINING:

  • BS/MS degree in neurobiology or related discipline
  • 8+ years Biotech/Pharma experience drug discovery experience in neuroscience

RESPONSIBILITIES INCLUDE:

  • Culture and maintenance of cell lines, primary neurons and iPSC-derived neurons
  • Stable cell line generation
  • Assessment of compound efficacy via immunocytochemical, biochemical and molecular biology techniques, such as immunostaining and immunoblotting
  • Interaction and collaboration with biology and chemistry team members to contribute to structure-activity relationship determination
  • Analysis of experimental data, addressing methodological problems in experimental protocols and results
  • Documentation, compilation, and interpretation of experimental data.
  • Presentation of data in oral and written reports in a clear and concise manner to supervisor and project teams
  • Management of laboratory notebook, databases and/or spreadsheets to compile and present results in a meaningful manner
  • Keeping up-to-date on relevant scientific literature

REQUIRED SKILLS AND ABILITIES:

  • Proficiency in basic lab techniques and principles of cell and molecular biology, biochemistry and neurobiology
  • Proficiency in culturing primary neurons and neuronal cell lines
  • Experience in assay validation, assay development and small molecule testing
  • Basic understanding of neurodegenerative diseases
  • Ability to work and problem-solve independently while under general supervision by the project leader

Location

New Haven, CT

Please send CV and cover letter to: careers@arvinas.com.

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Sr. Associate/Research Scientist, Formulation R&D

Arvinas is a pharmaceutical company focused on developing new small molecules ‒ known as PROTACs (PROteolysis TArgeting Chimeras) ‒ aimed at degrading disease-causing cellular proteins via proteolysis. Based on innovative research conducted at Yale University by Dr. Craig Crews, Founder and Chief Scientific Advisor, the company is translating natural protein degradation approaches into novel drugs for the treatment of cancer and other diseases. The proprietary PROTAC-based drug paradigm induces protein degradation, rather than protein inhibition, using the ubiquitin proteasome system and offers the advantage of potentially targeting “undruggable” as well as “druggable” elements of the proteome. This greatly expands the ability to create drugs for many new, previously unapproachable targets. 

The Research Scientist will serve as a core member of the development team and execute formulation strategy for Arvinas drug candidates. The incumbent will be responsible for executing exploratory research and development studies, as well as supporting clinical supply manufacture through in-house efforts and CDMOs. In addition, the successful candidate will support the in vivo group in preparing dosing solutions and troubleshooting vehicle failures.  He/She will work closely with in vivo biology, process chemistry, clinical supply logistics, and clinical to develop vehicles and formulation to advance assets into preclinical and clinical studies.  The incumbent will ensure all activities occur in compliance with the appropriate SOPs and regulations.

Responsibilities include research on and development of formulations to support enabling exploratory and pre-clinical animal studies, as well as clinical studies.  This will be accomplished through a blend of in-house and out-sourced activities.  In addition to a hands-on component, the incumbent will be responsible for preparing requests-for-proposals, and monitoring the activities of several formulation development and manufacturing organizations.  The incumbent will provide critical analysis of on-going development activities and continually assess the suitability of a particular formulation for its intended use. A key activity of this role will be the assembly/evaluation of pharmaceutical study data and drafting of the relevant sections of INDs and NDAs.

ESSENTIAL FUNCTIONS

  • Design, carry out, and interpret preformulation studies on new and potential drug candidates, with the purpose of defining their physicochemical and biopharmaceutical properties relevant to oral and parenteral administration
  • Develop fit-for-purpose formulations to enable exploratory and enabling animal studies
  • Provide technical expertise, and specialized knowledge in formulation development and drug product manufacturing to support the Arvinas portfolio of drug candidates.
  • Work closely with in-life groups to develop and prepare formulations suitable for use in drug discovery pharmacology, pharmacokinetic, and toxicology studies
  • Assist in the preparation of requests-for-proposals, selection of vendors, and monitoring the activities/emergent data of/from formulation development and manufacturing organizations.
  • Apply scientifically-driven thinking to the development of formulations and products which meet pre-determined product profiles.
  •  Evaluate data associated with characterization of drug products and stability testing and assess suitability of a drug product for an intended purpose.
  • Convert data on formulations/products into knowledge required for IND and NDA filings. Assist in drafting the relevant sections of these regulatory filings.
  • Works closely with peers on project teams to seamlessly and expeditiously advance Arvinas assets into the clinic

POSITION QUALIFICATIONS

  • BS/MS in Pharmaceutical / Medicinal / Physical / Analytical Chemistry
  • 6-10 years of experience in industrial drug development is required
  • Hands-on experience with formulation development/manufacturing
  • An understanding of basic medicinal chemistry and biopharmaceutical principles as they apply to drug discovery and development
  • A willingness to take on challenging problem statements and acquire/apply the skills necessary to address them
  • Ability to be proactive in identifying issues and hurdles that may hinder the effective implementation and/or progression of a study and resolve the issues in a timely and creative fashion
  • Experience with creating RFPs, and working with CDMOs for pre-formulation, formulation development, and manufacturing of drug product
  • Working knowledge of Good Manufacturing Practices (cGMPs) and Regulatory Guidance Documents as they relate to manufacture and quality testing of pharmaceutical products
  • Ability to effectively prioritize and deliver on tight timelines
  • Experience in communicating/presenting complex information to senior management
  • Ability to multi-task and manage several projects in parallel, paying attention to detail
  • Ability to forge cross-functional working relationships with internal and external project partners
  • Good oral and written communications skills
  • Experience in using computers and databases for data collection, compilation, analysis, and information dissemination
  • Proficient with MS Word, PowerPoint, Excel

Job Requirements – Personality

 

  • Conduct themselves in an ethical, honest and accountable manner
  • Ability to establish and maintain effective working relationships
  • Ability to work in a fast-paced, highly-motivated work environment
  • Entrepreneurial with self-starting personality; ability to prioritize and manage multiple responsibilities simultaneously
  • Enthusiastic desire to roll up sleeves and dig in. Confidence in own abilities to get things done.
  • Able to meet tight deadlines on multiple priorities.
  • Strong analytical skills with attention to detail and accuracy
  • Customer focused with strong team work, interpersonal and communication skills
  • Requirement to maintain a high level of confidentiality
  • Ability to develop solutions to problems and implement them.

Location

New Haven, CT

Please send CV and cover letter to: careers@arvinas.com.

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