Skillset: Sr Epi - Inflam-Liver Group. Hybrid trial adding controls to placebo group. CDisc Reqs ... or consulting environment. Master's degree in epidemiology, biostatistics, bioinformatics, or ...
Skillset: Sr Epi - Inflam-Liver Group. Hybrid trial adding controls to placebo group. CDisc Reqs ... or consulting environment. Master's degree in epidemiology, biostatistics, bioinformatics, or ...
Senior Bioinformatics Consultant information
What are the key skills and qualifications needed to thrive as a Senior Bioinformatics Consultant, and why are they important?
To thrive as a Senior Bioinformatics Consultant, you need advanced knowledge of bioinformatics, genomics, and statistical analysis, typically supported by a graduate degree in bioinformatics, computational biology, or a related field. Expertise in programming languages (such as Python or R), experience with next-generation sequencing (NGS) analysis tools, and familiarity with bioinformatics databases are crucial. Strong problem-solving, effective communication, and project management skills help you collaborate with cross-disciplinary teams and translate complex data into actionable insights. These skills ensure the delivery of robust data-driven solutions to scientific and clinical partners, driving impactful research outcomes.
How does a Senior Bioinformatics Consultant typically collaborate with research teams and stakeholders across projects?
As a Senior Bioinformatics Consultant, you will frequently work closely with multidisciplinary teams, including biologists, clinicians, and software engineers, to interpret complex biological data and provide actionable insights. This collaboration involves regular meetings to discuss project goals, progress updates, and troubleshooting data analysis challenges. You may also be responsible for translating technical results into clear, non-technical reports for stakeholders, facilitating decision-making. Effective communication and project management skills are crucial, as you often coordinate tasks across multiple ongoing projects.
What does a Senior Bioinformatics Consultant do?
A Senior Bioinformatics Consultant leverages advanced computational and analytical skills to interpret complex biological data, often working with genetic, genomic, or clinical datasets. They advise researchers, pharmaceutical companies, or healthcare organizations on data analysis strategies, workflow optimization, and the implementation of bioinformatics tools. Their responsibilities may include designing experiments, developing custom software solutions, and translating scientific findings into actionable insights. Additionally, they often mentor junior team members and serve as a bridge between biological scientists and IT professionals.
What is the difference between Senior Bioinformatics Consultant vs Bioinformatics Analyst?
| Aspect | Senior Bioinformatics Consultant | Bioinformatics Analyst |
|---|---|---|
| Required Credentials | Bachelor's/Master's in Bioinformatics, Computer Science, or related; experience in consulting | Bachelor's or Master's in Bioinformatics, Biology, or related; entry to mid-level experience |
| Work Environment | Consulting firms, biotech companies, research institutions | Research labs, healthcare organizations, biotech firms |
| Employer & Industry Usage | Used in client-facing roles, project management, strategic planning | Data analysis, report generation, data management |
The main difference is that Senior Bioinformatics Consultants focus on client advisory, project leadership, and strategic solutions, often working across multiple projects and clients. Bioinformatics Analysts primarily handle data analysis, interpretation, and reporting within organizations. Both roles require strong bioinformatics skills, but the consultant role emphasizes communication and project management.
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Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 19 days ago
Job description
Director, Epidemiology RWE - Pharma Co
Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.
Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver - for one another, our customers, and, most importantly, for those in need.
Discover what your 25,000 future colleagues already know:
Why Syneos Health
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
We are committed to building an inclusive culture - where you can authentically be yourself. Central to this is our purpose - Driven to Deliver - which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone's life.
We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.
Job Responsibilities
*This role is open to candidates who live in the US with no sponsorship needs.
Skillset: Sr Epi - Inflam-Liver Group. Hybrid trial adding controls to placebo group. CDisc Reqs, PharmaCo Epi
- Clinical background - preferred
-PHD Required
Required Experience
Lead development of study protocols, analysis plans, and study reports to answer research questions of priority to RWE
Lead, design, and manage epidemiological, biomarker and/or data science projects
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Lead, plan, design, and conduct analyses for internal and external decision making (e.g., responses to regulatory authorities, rapid analyses of safety queries)
Lead the identification of fit-for-purpose data for the timely execution of the RWE strategy
Constructed cohorts using RWD sources (e.g., claims, EHR) and evaluate key variables, including diagnosis and procedures codes, and plan validation studies as needed
Contribute to the communication of observational research results and methods, including development of pertinent sections of regulatory documents, reports, publications, white papers
Support the effective communication of study/analysis results to support internal and external decisions
Coauthor abstracts and manuscripts for external dissemination of methodologic study results
Contribute to the development of processes and training aimed at increasing the efficiency, quality, and impact of functional activities
Technical Expertise
o Observational research methods (both Primary and Secondary), deep knowledge of biostatistics and analysis methods, understanding of regulatory processes,
o Ability to design studies independently, (ie ability to translate research questions to create study design)
Subject Matter Expertise
o Provide subject matter expertise and conduct analyses for descriptive and comparative research using RWD (examples include claims, EHR, PRO/COA, registry data) for methodologic research questions
Minimum Qualifications
PhD in Epidemiology, Biostatistics, Psychometrics, or related field with a minimum of four (4) years of relevant post-doctoral experience, preferably in pharmaceutical industry, biotechnology, or consulting environment. Master's degree in epidemiology, biostatistics, bioinformatics, or relevant scientific field, plus 7-9 years of experience in lieu of PhD may be acceptable.
Deep understanding of observational research methods and experience to support the design and conduct of observational research, including protocol, statistical analysis plan, and study report development
Extensive knowledge of secondary data sources and experience with secondary data analysis, including electronic medical record and/or medical claims databases
A record of scientific publications demonstrating expertise in observational study design, analysis, and interpretation is preferred
Demonstrated ability to function with an increasing level of autonomy and to develop productive cross-functional collaborations in a matrix environment
Ability to manage priorities and performance targets
Experience in leading drug development project for 2+ years for therapeutic area of assignment preferred
At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.
Salary Range:
$118,700.00 - $207,800.00The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate's qualifications, skills, competencies, and proficiency for the role.
Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
http://www.syneoshealth.com
Additional Information
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.