Associate Scientific Director Resume Sample
Dennis Kihn
62087 Hessel Highway,
New York,
NY
+1 (555) 335 5095
Work Experience
Associate Scientific Director
12/2016
-
PRESENT
San Francisco, CA
- Approve validation reports and technical reports for molecular pathology assays. Contribute to relevant regulatory documents when required
- Approve assay transfer quality for assays transferred to external contract research laboratories and companion diagnostic partners in support of clinical development and companion diagnostic development
- Provide scientific direction and expertise in pathology for both non-clinical and clinical study experiments, including writing relevant sections of clinical trial protocols
- Maintain familiarity with CAP and CLIA regulations
- Maintain familiarity with relevant regulatory requirements surrounding companion diagnostic development
- Keep current with technological developments that impact molecular pathology
- Board certification in Anatomic Pathology is required
- Strong experience in identifying and adopting new genomic technologies and techniques in support of an evolving business domain
- Analyze business needs and act decisively; demonstrated ability to make prudent decisions to achieve desired outcomes
Associate Director, Scientific Affairs
04/2010
-
08/2016
Los Angeles, CA
- Demonstrated experience and influence in the strategy, design and implementation of projects and program deliverables
- Willingness to work in a matrix environment and to value and promote the importance of teamwork
- Proven achievement in leading, managing and motivating empowered teams
- Negotiate with respect and influence to achieve results
- Responsible for the strategic and operational delivery of client programs and projects to time lines, quality expectations and regulatory requirements
- Oversee or serve as the primary source of scientific support for the design, analysis, reporting, and presentation of ‘omic analyses for all phases of drug development
- Responsible for authoring, contributing to or reviewing documents such as technical reports, analysis plans, sections of regulatory documentation, scientific publications, abstracts, posters
Associate Director, Scientific Computing
08/2007
-
01/2010
Phoenix, AZ
- Maintain a strong working knowledge of relevant fields such as biostatistics, bioinformatics, computational biology, computational programming, statistical genetics, drug discovery and development
- Develop and maintain a positive relationship with internal and external clients and scientists
- Provide training and scientific support and advice to relevant PAREXEL staff
- Attend client meetings and represent Genomic Medicine as needed
- Participates as a member of the Due Diligence (DD) team from kick-off through close-out, to evalu-ate target opportunities with a CMC sub-team, looking for risks and opportunities in the area of API and Finished Product characterization/evaluation and any other aspects based on QbD which could impact the successful development, filing and commercialization of the target asset
- Prepares DD reports to summarize the findings into a concise evaluation of possible risks and op-portunities, and a prioritized, actionable plan and mitigation strategy
- Write editor’s notes and introductions for, and summary statements of, content received from faculty/authors and medical writers
- Provide scientific expertise and guidance to creative, strategy, editorial, and account management teams; serve as trusted internal resource
Education
Southwest Minnesota State University
2002 - 2007
Science's Degree in Chemistry
Professional Skills
- Expertise in use of Microsoft Office applications: STRONG skills in Microsoft Word and PowerPoint
- Excellent interpersonal skills with the ability to interact with account teams, other writers, editors, physicians and clients
- Excellent interpersonal, communication, analytical, managerial, and organizational skills
- Has strong leadership skills and acumen
- Excellent written, communication skills and recognized knowledge and expertise in the field of anatomic pathology is required
- Excellent communication skills and the drive to build client and team relationships
- Relevant experience or equivalent in a virology-related role. Previous management experience required
How to write Associate Scientific Director Resume
Associate Scientific Director role is responsible for design, reporting, retail, training, recruiting, oncology, manufacturing, research, digital, modeling.
To write great resume for associate scientific director job, your resume must include:
- Your contact information
- Work experience
- Education
- Skill listing
Contact Information For Associate Scientific Director Resume
The section contact information is important in your associate scientific director resume. The recruiter has to be able to contact you ASAP if they like to offer you the job. This is why you need to provide your:
- First and last name
- Telephone number
Work Experience in Your Associate Scientific Director Resume
The section work experience is an essential part of your associate scientific director resume. It’s the one thing the recruiter really cares about and pays the most attention to.
This section, however, is not just a list of your previous associate scientific director responsibilities. It's meant to present you as a wholesome candidate by showcasing your relevant accomplishments and should be tailored specifically to the particular associate scientific director position you're applying to.
The work experience section should be the detailed summary of your latest 3 or 4 positions.
Representative Associate Scientific Director resume experience can include:
- Educate creative, strategy, editorial, and account teams on scientific aspects of assigned accounts, demonstrating strong understanding of the relevant therapeutic area and market environment
- Review promotional materials to add value and assure scientific accuracy and strategic alignment, and to ensure quality output that helps to build the scientific foundation for pharmaceutical and biotech brands
- Guide, review, and assist copywriters on appropriate promotion language in support of client messaging that is consistent with regulatory guidelines associated with product indication
- Draft outlines or clinical descriptions that guide copywriter efforts within a scientifically rigorous framework that is strategically sound and consistent with client expectations
- Proven drug hunting experience and advancing projects from concept to clinic is required
- Supervise team of scientific personnel with varying skill level, including other supervisors
Education on an Associate Scientific Director Resume
Make sure to make education a priority on your associate scientific director resume. If you’ve been working for a few years and have a few solid positions to show, put your education after your associate scientific director experience. For example, if you have a Ph.D in Neuroscience and a Master's in the same sphere, just list your Ph.D. Besides the doctorate, Master’s degrees go next, followed by Bachelor’s and finally, Associate’s degree.
Additional details to include:
- School you graduated from
- Major/ minor
- Year of graduation
- Location of school
These are the four additional pieces of information you should mention when listing your education on your resume.
Professional Skills in Associate Scientific Director Resume
When listing skills on your associate scientific director resume, remember always to be honest about your level of ability. Include the Skills section after experience.
Present the most important skills in your resume, there's a list of typical associate scientific director skills:
- Skilled in several programming languages and tools (R, PERL, PYTHON, etc) with very strong programming skills in R
- Effectively prioritize and attend to numerous ongoing projects on defined timelines
- Excellent skills using MS Office and Adobe Acrobat
- More than 10 years of relevant experience in translational neurophysiology research and at least 5 years of industry experience
- Effectively manage staff and deliver clear instructions and feedback routinely and as part of the review process
- Prior Medical/Scientific Liaison experience
List of Typical Experience For an Associate Scientific Director Resume
1
Experience For Associate Director, Scientific Affairs Resume
- Assist in new business development by conducting background research, creating educational materials for the internal team, and contributing to the preparation of new business proposals
- Excellent effectiveness and clarity in oral and written communication
- Demonstrates independent thought and ability to exercise judgment to influencing design and implementation of projects and program deliverables
- Experience in the pharmaceutical industry or equivalent; substantial understanding of relevant therapeutic area required
- PhD in Immunology/Pharmacology with at least 7 years of pharmaceutical industry experience with progressively advanced responsibilities is required
- Previous supervisory experience of PhD level and non-PhD-level scientists is required
- Solid background in Immunology/ Pharmacology is required
- Demonstrated Focus on Patients interest
2
Experience For Associate Scientific Director, GI DDU Resume
- Experience in the creation of analysis workflows and pipelines
- Demonstrated understanding of PK, PD, PK/PD, ClinPharm, and Translational Medicine
- Excellent knowledge of scientific computing and genomic data sciences
- Demonstrated expertise with open source genetic software such as GATK, SAMtools, VCFtools, PLINK
- Knowledge and experience of common bioinformatics databases, resources and tools
- Strong background in viral vectors (AAV, Lenti, etc) is required
- Experience with cell based virology methods is required
- Therapeutic area experience in Cardiovascular Disease/Thrombosis, Hematology/Oncology, Immunology, or Neurosciences
3
Experience For Associate Scientific Director, Toxicology Resume
- In-depth understanding of clinical trial design and statistics, and ability to develop and present complex data in simple graphical formats
- With minimal guidance from ClinPharm TA Head, develop and implement Model-Based Drug Development (MBDD) ClinPharm plans and strategies for products in all stages of Drug Development
- Perform and / or liaise with AM&S on modeling and simulation of dose- and exposure-response (PD, toxicity, and safety endpoints) to guide starting dose, dose regimen, and dose range for FIH, MAD, PoC, Phase 2b, and Phase 3 trials
- Work collaboratively with key functional partners and apply quantitative ClinPharm tools to guide NME selection, dose / dose regimen selection, predict clinical response and study outcomes, and to optimize study design
- With minimal guidance from ClinPharm TA Head, provide appropriate dosing recommendations for special populations (eg, drug interaction, food effect, pharmacogenomic effect, pediatric, elderly)
- With minimal guidance from ClinPharm TA Head, prepare ClinPharm contributions to regulatory documents including IBs, End of Phase 2a / 2 meetings, NDA / MAA submissions, postapproval filings, and responses to regulatory questions
- Represent ClinPharm on Clinical Teams and Compound Development Teams, where appropriate, and oversee activities of Phase 1 Working Group
- As requested, participate in the evaluation of potential in-licensing opportunities
- Liaise with key functional partners to provide product differentiation strategies based on a compound’s key ClinPharm attributes
4
Experience For Associate Director, Scientific Computing Resume
- With oversight, contributes to the development of brand strategies
- Contributes to the development of and leads the execution of the Medical Education / Advisory Board & EE Engagement Plan generation in line with TA plan. Lead the individual (US or Global) Conference planning and execution
- Generates clinical and scientific data (DOF) as needed to support external communication (RRTI)
- Responsible to manage budget for assigned projects
- Aligns Medical education and scientific initiatives with Sci Comm Platform. Informs Investigator Initiated Study (IIS) strategy and can act as Docent for IISs
- Actively contributes to the development of a TA EE Engagement Plan
- Participation in design and execution of clinical trial safety, product safety and risk management plans. Track RMP implementation
- Develop original clinical content (monographs, newsletters, slide decks, etc) across multiple delivery platforms―print, live, and digital (web, tablet, and mobile) ― in accordance with established budgets, timelines, and strategic objectives
- Repurpose client-supplied materials for use in custom promotional and educational programs for healthcare professionals
5
Experience For Associate Scientific Services Director Resume
- Provide strategic, technical and scientific leadership for electrophysiology biomarker development
- Situational leadership of Global Product Teams (GPT) in the neurophysiology biomarker selection for first-in-human studies, provide pharmacologic and pharmacodynamic rationales and translational approaches for early clinical protocols
- Oversee the design and implementation of neurophysiology biomarker research in clinical trials and monitor the scientific quality of electrophysiology clinical assay data
- Work independently, manage and mentor scientists doing cutting edge research, design experiments, interpret data, troubleshoot and suggest next steps, detail-oriented with strong organizational skills
- Experience leading/ advancing drug discovery programs in immune-mediated diseases is required
6
Experience For Associate Director, Scientific Licensing Resume
- Develop original clinical content (monographs, newsletters, slide decks, etc.) across multiple delivery platforms―print, live, and digital (web, tablet, and mobile) ― in accordance with established budgets, timelines, and strategic objectives
- Experience in medical content development (monographs, newsletters, slide decks, etc.) across multiple delivery platforms (print, digital, and live programs) within an organization serving pharmaceutical clients
- Design, supervise, and interpret R&D and GMP studies. Provides appropriate resources to team to conduct studies
- Assumes responsibility for direct reports and team. Directs and leads team to stay on track to meet project deadlines. Communicates progress to manager regularly
- Conducts regular staff meetings and one on one meetings with each direct report
7
Experience For Associate Scientific Director Resume
- Oversees assay transfers between own team and Operations
- Authors technical documents, procedures, policies, SOPs, & risk assessments, as needed
- Implement innovative solutions and propose new technologies in support of multiple projects
- Lead cross-functional teams in effort to solve organizational and process problems
- Responsible for ensuring departmental compliance to REES/ELPRO monitoring and response procedures. Provides appropriate resources and expectations to team for responding to alarms
- Assess team resourcing needs. Present to headcount committee
- Provide leadership, direction, and mentoring to ClinPharm STO staff
8
Experience For Associate Director, Scientific Affairs Resume
- Complies with all internal and external regulations and policies and procedures. Ensures safety and compliance of laboratory and team
- Tracks progress of department's change controls. Ensures project goals are met and change controls are closed out in a timely manner
- Investigates, responds and/or approves equipment OOTs
- Represents the company in key client meetings and outside conferences
- Travels with other WuXi AppTec staff to visit clients as appropriate
9
Experience For Associate Scientific Director, GI DDU Resume
- Interacts with CROs at multiple levels, including: transferring methods developed at Janssen, monitoring CRO validations, and the monitoring of immune endpoints during both GLP and non-GLP studies
- Active member of various Takeda committees and task forces which define the processes for developing and implementing Global Takeda standards that are used in clinical development, post-marketing surveillance, and Pharmacovigilance process in order to promote the consistency of data throughout the Takeda group companies
- Represents clinical science and leads internal task forces as well as global cross-functional teams as appropriate
- Bachelors required with 15 years of clinical research experience within the pharmaceutical industry, CRO health-related consulting company, or biomedical/clinical experience within academia (or a combination of afore mentioned) and professional license
- Responsible for the consistency, quality, compliance, and timeliness of ClinPharm input into Phase 1 to 3 protocols, ClinPharm analyses, Development Plans, and relevant sections of IBs, CSRs, regulatory, and other documents in accordance with applicable SOPs, guidelines, and regulatory requirements
10
Experience For Associate Scientific Director, Toxicology Resume
- Contribute to process-related initiatives within ClinPharm department
- Strengthen partnerships, teamwork, and communication across functional units within one’s area of responsibility
- Independently leads development of PS strategy and plans for multiple programs
- Projects (and is recognized for) expertise in cross functional/divisional team leadership and communication
- Leads and influences functional/divisional strategy and initiatives
List of Typical Skills For an Associate Scientific Director Resume
1
Skills For Associate Director, Scientific Affairs Resume
- Strong leadership skills with highly collaborative instincts
- This role requires excellent communication and interpersonal skills, a high level of organizational ability and attention to detail
- Demonstrated expertise working in UNIX/LINUX environment. Experience with cloud computing
- Experience or strong knowledge of pharmacogenomics or pharmacogenetics
- Exceptional organizational skills and the ability to work independently
2
Skills For Associate Scientific Director, GI DDU Resume
- Experience in pharmaceutical/biotechnology research management or related experience in drug development is required
- Good working knowledge of developing educational content for medical professionals
- Demonstrated expertise with R, python, shell scripting or other programming languages and tools
- Proven working knowledge of current GMP/GCP regulations
- Experience in clinical or pharmaceutical setting with background in Medical Affairs or Clinical Research
- Typically 8 yrs experience in the pharmaceutical industry or equivalent; substantial understanding of relevant therapeutic area required
- Knowledge of regulatory requirements impacting Genomic Medicine and drug development is strongly desired
- Demonstrated proficiency in computational programming
3
Skills For Associate Scientific Director, Toxicology Resume
- Relevant experience in bioinformatics, computer science, engineering, statistics, or mathematics
- Experience with various ontologies and controlled vocabularies and coding systems
- Previous experience managing external partnerships (CRO’s) is required
- >3-4 years medical writing/medical communications experience
- PhD in Biological Science or science related field or equivalent experience
- In-depth knowledge and experience of common bioinformatics and genomic databases, resources and tools
- Demonstrated proficiency in the evaluation, recommendation and implementation of analytical methods
- Understanding of ACCME policies and standards
4
Skills For Associate Director, Scientific Computing Resume
- Leading expert in field of expertise and broad knowledge across technical areas. Lead cross-functional investigations
- Leadership – demonstrable ability to provide ongoing feedback and coaching to employees and to guide other leaders within the department in doing the same
- Assist with growing client relationships by demonstrating mastery of the brand's science and by helping to shape medical strategy as needed
- Comply with institutional certifications and requirements in a BSL-2 environment, including shipping regulations for infectious agents
- Understand business offerings and identify opportunities for organic account growth, including cross-selling, and new business
- Knowledge of programming languages and working in a HPC linux environment
5
Skills For Associate Scientific Services Director Resume
- Serves as analytical lead representing Analytical Development and Laboratory Operations on multiple manufacturing core teams for highly complex programs
- Interfaces with BD and Sales team regularly. Assists with custom testing quotes and the analytical portions of manufacturing quotes
- Lab equipment owner. Responsible for determining departmental equipment needs and justifying CapEx
- Leads Development Working Groups and ensures alignment with the global strategy
- Support management of IISR research by conducing protocol reviews, etc
- Provide expertise and support to Medical Communication team to develop medical communications, publications, and training plans
6
Skills For Associate Director, Scientific Licensing Resume
- Client focused approach to work ethic. Capable of handling confidential information and data
- Self-motivated and proactive with a flexible attitude to work assignments and new learning
- Lead and execute development of content including data analysis for a wide range of complex projects, with minimal review/direction
- Knowledge of translating genomic data into clinically relevant results
- Serve as the team scientific representative during client medical-legal-regulatory review of promotional materials
- Contributes to the generation of MI communication content and supports training on Medical Information (MI) materials
- Medical Review (MR) Training on label, clinical data and disease state
7
Skills For Associate Scientific Director Resume
- Assists Sr. Director and VP with the departmental strategical planning and growth of their team
- Quickly develop competency in use of Medscape and WebMD software applications and content development tools: Workfront, Box
- Proficient in the application of project management knowledge, skills, tools (e.g. Microsoft Project), and techniques for complex multidisciplinary programs and initiatives
- Leadership - develops and uses knowledge and interpersonal skills to influence and guide internal and external stakeholders towards the accomplishment of program and cross-divisional goals and objectives; adapts well to varied team dynamics and manages others team members in a respectful manner
- Risk Management -ability to identify/mitigate technical, budgetary, and schedule risks to multiple programs and propose appropriate risk response strategies. Ability to identify gaps in PS technology/trends and influence change/improvements to affected areas/processes
8
Skills For Associate Director, Scientific Affairs Resume
- Communication -ability to expresses one’s self clearly and concisely to key stakeholders and functional management; documents issues and/or concerns concisely and comprehensively; adjusts style, language and/or terminology appropriate for the audience. Can represent PS viewpoint at divisional level
- Resource Management -ability to anticipate and manage internal and external resource needs (people, information, technologies, time, and capital)
- Analyze and synthesize complex information from multiple sources
- Efficiently prioritize multiple tasks and provide effective direction to others; can quickly evaluate the resources necessary to accomplish a goal and put those into action
- Experience in robust product development and QbD principles
- Therapeutic area expertise knowledge relevant to disease states and mechanism of action
9
Skills For Associate Scientific Director, GI DDU Resume
- Work independently, take initiative, lead and complete tasks to deadlines
- Executes and implements the regional team strategy producing the Clinical Development Plan and Clinical Protocols. Recommends scope, complexity, and size of a program which impacts multimillion dollar budget decisions
- Provides scientific expertise to functional area representatives GCDT on disease state, study design, and scientific rationale in clinical studies for compounds within therapeutic area
- Provides on-going critical evaluation of the development strategy to maintain a state-of-the-art development plan that is competitive and consistent with the latest regulatory requirements, proactive identification of challenges, and development of contingency plans to meet them
- Authors/supports publication and presentation of clinical and nonclinical data in support of Takeda developed or licensed compounds
- Leads Cross Portfolio alignment and coordination of KOL engagement, congress planning and research collaboration across the Medical Affairs- Clinical Development and Commercial Organization for products
10
Skills For Associate Scientific Director, Toxicology Resume
- Work with GMA Leads to develop GMA plans and strategies
- Obtain organizational endorsements of medical affairs initiatives
- Develop gap analysis for relevant post launch clinical date and design solutions to address
- Participate in the development of IISR strategy
- Present disease and pipelines overviews
- Provide expertise and support for advisory boards
List of Typical Responsibilities For an Associate Scientific Director Resume
1
Responsibilities For Associate Director, Scientific Affairs Resume
- Investigates and develops novel experimental methods/technologies, contributes to improvement of existing methods and develops new in vitro/in vivo models to enhance our understanding of potential immunotoxicology risk and translatability to humans in the clinic
- Maintains strong scientific network in academia and the pharmaceutical/biotechnology industry to enable external interactions, consulting and recruiting
- PharmD/PhD with 4+ years pharmaceutical industry experience
- Demonstrated expertise with relational databases, SQL, and web development frameworks
- Maintains an industry leading expertise in Immunotoxicology
- Provide computational support for external collaborations and consortia involving human cohorts
- Provide Pathology support for in-licensing activities for the therapeutic area
- Participates in communication of information and data presentation in oral and written format both in-house and at appropriate external forums
- Represents the organization to senior management and peer groups within Janssen and Johnson & Johnson
2
Responsibilities For Associate Scientific Director, GI DDU Resume
- Be a mentor/coach to key scientific staff and guide/enable their career/professional development
- Responsible for the development of all employees within the department by supporting the development of Human Resources Planning (HRP) programs including management development and training to meet current and future business needs
- Provide an environment, which encourages the company's commitment to equal employment opportunity and the value of a diverse work force
- Established expertise in Immunotoxicology is required
- Expertise in immunological techniques (e.g. flow cytometry, immunoassays) is required
- Knowledge of GLPs is required
- Develop original clinical content (monographs, newsletters, slide decks, etc.) across multiple delivery platforms ― print, live, and digital (web, tablet, and mobile) ― in accordance with established budgets, timelines, and strategic objectives
3
Responsibilities For Associate Scientific Director, Toxicology Resume
- Provide expertise and data analyses for human genetic databases. Drive ontology decisions in order to harmonize phenotypes to enable data analyses across multiple cohorts from different countries
- Provide medical expertise for genetic, genomic or epigenetic studies applied to AbbVie clinical trials
- Collaborate with Medical Directors in Clinical Development as well as other Scientific Directors within the GRC to identify relevant questions and design studies related to drug response or disease etiology, with a focus on the computational aspects of the projects
- Ensure consistent on time delivery, to Study Directors, of high quality Pathology data and Pathology reports for all Preclinical Toxicology studies to meet project goals and milestones
- Utilize a broad knowledge of pathophysiology across veterinary species to provide scientific leadership in collaboration with the functional representative (PCDL) on Discovery/Development and/or cross sector research project teams
- Collaborate with stakeholders at all levels to optimize processes within Pathology to maximize efficiency and drive project progression; demonstrate and introduce innovation in both local and global components of the drug discovery and/or development process
4
Responsibilities For Associate Director, Scientific Computing Resume
- Work cross-functionally in a matrix environment and understand the ways of working across different geographies and cultures
- Provide leadership, scientific direction and guidance to the identification and development of novel biomarkers of target organ toxicity
- Interacts with research division based on pertinent clinical and development expertise to provide knowledge / understanding of market environment in line with status as TGRD scientific content matter expert for assigned compounds
- MD., or PharmD., or PhD. Required
- Ph.D. in toxicology or related discipline (immunology, pharmacology, cell/tumor/molecular biology, or related field) with at least 6 years of pharmaceutical/biotechnology research management or related experience in drug development is required
5
Responsibilities For Associate Scientific Services Director Resume
- Experience interacting with Regulatory Agencies including experience in authoring toxicology sections of regulatory documents (e.g. IBs, INDs, EOP2, Scientific Advice, BLA) is required
- Some travel (domestic and international) is required dependent on project needsToxicology Research
- Experience in the pharmaceutical or diagnostic industry with professional responsibility driving completion of strategic initiatives and tactical plans with a collaborative approach. Demonstrated success to leading cross-functional teams to achieve business strategic goals
- Expertise in conducting literature searches and concisely summarizing findings
- Work in a fast-paced, deadline-driven, team-oriented environment
- Demonstrated understanding of MBDD, BCS, BDDCS, and biostatistics principles and tools and demonstrated ability to apply these tools to enable rational and efficient drug development
- Proficient in the use of Microsoft Office suite of software products
- Interactions normally require the ability to gain cooperation of others, conduct presentations of technical information concerning specific projects and schedules, etc
6
Responsibilities For Associate Director, Scientific Licensing Resume
- Represents AbbVie at external meetings including investigator meetings, scientific association meetings, etc
- Works with some supervision and guidance. Exercises judgment within well-defined practices and policies
- Demonstrated expertise in the handling, processing and analysis of large volume genetic, genomic, or other omics data (NextGen sequencing, genotype arrays, metabolomics, proteomics, etc.)
- Expertise with clinical trial conduct in pharmaceutical industry, CRO or academia
- Demonstrated proficiency in the processing, management and analysis of large volumes of ‘omic data (NextGen sequencing, genotype arrays, metabolomics, proteomics, etc.)
7
Responsibilities For Associate Scientific Director Resume
- Publication record in peered review journals
- Board certified by American/European College of Veterinary Pathologists (ACVP or ECVP) is required
- Clearly communicates portfolio development to stakeholders
- Recognized expertise in Neurophysiology techniques development and Translational Medicine as demonstrated by publications, regulatory submissions and/or national or international presentations
- Promote J&J Credo
- BS + 16 years
- MS + 12 years
8
Responsibilities For Associate Director, Scientific Affairs Resume
- Pharma D + 11 years
- PhD + 10 years
- A passion for science and medicine, with a proven track record of communicating medical advances to different audiences and getting up to speed quickly on new therapeutic areas
- Independently and accurately incorporate strategic concepts into projects as well as guide others to do so
- Experience with large-scale research projects involving next generation DNA sequencing data (e.g. whole exome and whole genome) in conjunction with results from informatics and wide array of molecular biology strategies
9
Responsibilities For Associate Scientific Director, GI DDU Resume
- Foster research relationships with key cancer research centers globally and in US
- Lead Medical Affairs clinical research studies, including phase 4 studies, registries, meta-analyses and retrospective studies Provides scientific expertise to functional area representatives on disease state, study design, and scientific rationale in clinical studies for compounds within therapeutic area
- Interprets data from an overall scientific standpoint
- Collaboratively interacts with scientists from alliance partners
- Leadership – demonstrable ability to use confidence, decisiveness and a willingness to listen to, influence and engage others in the accomplishment of functional goals
- Communication – ability to articulately communicate ideas and data both orally and in writing. Excellent interpersonal skills, strong sense of collaboration, and excellent oral and written communication skills
- Analytical Skills – ability to analyze a wide variety of medical and scientific data including financial figures and market research data to make professional management decisions
10
Responsibilities For Associate Scientific Director, Toxicology Resume
- Business Process Acumen - ability to apply the knowledge of Takeda’s core business capabilities to help the organization meet its goals and desired outcomes
- Strategic Approach – ability to predict broad-based changes in business partner environment and translate them into functional strategies to continually meet business partner needs
- Pharmaceutical Industry Acumen - ability to develop and implement business solutions based on trends, opportunities, needs, and market direction within the pharmaceutical industry; ability to manage and adapt to the changing dynamics of the pharmaceutical industry in the context of Takeda’s business needs and objectives
- Leads/represents PS on multiple cross-divisional governance and development teams while providing strategy and accountability for PS deliverables
- Provides strategic scientific leadership and program management for multiple global PS development teams
- Identifies and communicates project or program risks and provides risk response strategies in a timely manner to appropriate stakeholders and PS management
- Lead/participate as functional expert in divisional and cross-divisional initiatives
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