9,178 Scientific jobs in the United States

**Duration: 12 Months Contract**
**Summary**
This position will contribute analytical and technical support for nitrosamines and impurities analysis.
**Responsibilities and Duties**
+ Conduct nitrosamines and impurities evaluations (routine and non-routine) by performing chemical analysis utilizing LC/MS/MS and associated wet chemistry and sample preparation techniques.
+ Conduct chemical analyses and preparation, including solid-phase extraction (SPE) and liquid-liquid extraction (LLE) in support of nitrosamines studies.
+ Perform experiments specifically for nitrosamines and E&L analysis, within specified timelines.
+ Operate, maintain, and troubleshoot MS instrumentation.
+ Participate in investigations that correspond to atypical or out-of-specification/out-of-trend results.
+ Independently plan and execute method development activities utilizing LC/MS/MS.
+ Generate scientific sound experimental data following written procedures including protocols and standard operating procedures (SOPs).
+ Independently author and contribute to experimental protocols, summaries, and technical reports.
+ Document and review laboratory work using an electronic laboratory notebook per Baxter's good documentation practices (GDP) and general good laboratory practices (GLP).
+ Follow Quality Manual, SOPs, and Environmental Health, Safety & Sustainability (EHS&S) guidelines in day-to-day activities, to ensure proactive compliance and continuous improvement.
+ Provide support to maintain a compliant, safe, and clean working environment/laboratory.
+ Evaluate analytical results, identify trends, exceptions, and interpretation of results relative to product requirements, definitions, and/or project goals.
+ Competent in interpreting analytical data and presenting in a form that is suitable for a diverse audience.
+ Communicate clearly with management, peers, cross-functional teammates, and non-technical audiences by openly sharing project status and hurdles and seeking input from other team members.
**Qualifications:**
+ To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The following knowledge, skills, and/or abilities are required:
+ Extensive hands-on experience with mass spectrometry analysis; specifically, MS/MS via HPLC or UHPLC tandem with APCI or ESI ionization. Experience with MassHunter preferred.
+ Required knowledge and demonstrated experience of analytical chemistry with relevant laboratory skills (hands-on experience with wet chemical techniques and instrumental analysis).
+ Possesses analytical problem-solving mindset, high learning agility, innovative experimental attitude along with good presentation skills.
+ Strong written and verbal communication skills in English.
+ Provide and accept critical feedback from others in a constructive manner.
+ Demonstrates an inclusive attitude and an ability to collaborate with team members and cross-functional team members for project deliverables.
+ Ability to objectively assess, organize, and clearly communicate information.
+ Ability to plan and complete the assigned work to meet project deliverables in a timely manner.
+ Proficient in Microsoft Office applications(Excel, Word, Outlook)
**Education and/or Experience:**
+ PhD with 0-3 years' experience, or a master's with 3-5 years' experience, or a bachelor's with 5-7 years' experience in a chemistry related field.
+ Analytical or organic chemistry preferred.
**About US Tech Solutions:**
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ( .
US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about.
**Job Summary**
The Operations Specialist - Animal Logistics is responsible for the management of oversight of animal colonies, which includes assignment of study reservations, monitoring of census levels, and coordination of routine animal monitoring.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
+ Responsible for the assignment of reservations against animals held in stock colony.
+ Responsible for ensuring census levels are maintained at a suitable level which supports study demand.
+ Communicates census needs or challenges with line management in a timely manner.
+ Works creatively and collaboratively with stakeholders to ensure efficient and optimal use of stock animals.
+ Keeps clear and precise records at all times to ensure that stock animals are used appropriately, especially with consideration of washout periods.
+ Works to coordinate the acclimation/habituation of all animals for appropriate study use.
+ Tracks use of stock animals such that they are used for an appropriate period of time and offers recommendations for retirement as necessary.
+ High degree of computer competency (e.g., Smartsheet, PowerBI, Laboratory Information Management System).
+ Responsible for all record keeping associated with stock animals.
+ Ensures all records are maintained in a detailed and organized fashion such that they are inspection/client ready at any time.
+ Ensures all stock animals are maintained for health and habituation needs to ensure prompt assignment to study.
+ Is capable of collaborating with multiple stakeholders and troubleshoot through complex scheduling demands.
+ Review documentation of functions performed as part of colony management.
+ Act as a back up to for departmental scheduling, inclusive of training for staff
+ Support inter-site scheduling needs.
+ Coordinate and prepare animal arrival.
+ Perform all other related duties as assigned.
**Job Qualifications**
+ Education: High school diploma, General Education Degree (G.E.D.), required. Bachelor's degree (BA/BS) or equivalent in biological science, preferred.
+ Experience: Minimum 2 years of applicable CRO experience in in-vivo operations or census/inventory management.
+ An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
+ Certification/Licensure: None, unless required by local government.
+ Excellent written and verbal communication skills.
+ Ability to manage multiple tasks and priorities to achieve goals.
+ Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
+ Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
+ Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
+ Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
+ Ability to work under specific time constraints.
PHYSICAL DEMANDS:
+ Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
+ Must be able to perform laboratory procedures, which require, talking, hearing, standing, or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
+ Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.
WORK ENVIRONMENT:
+ Work in a research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from moderate to loud.
+ The employee regularly works with live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
+ The noise level in the work environment ranges from low to high depending upon the species housed.
**About Discovery**
Discovery from Charles River is industry-proven in the successful development of novel therapies, with over 350 patents and 80 preclinical drug candidates delivered to our sponsors in the past 17 years. Backed by more than 650 scientists, our comprehensive, integrated portfolio employs the latest technology and platforms to provide chemistry, biology, and pharmacology services that support clients from the earliest stages of hit identification all the way through to IND. Our client-focused, collaborative approach creates true partnerships that anticipate challenges, overcome obstacles, and move us forward together on the journey of getting new drugs to market.
**About Charles River**
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.
At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.
229692

Our client is seeking an accomplished Senior Scientific Research Lead to spearhead groundbreaking research initiatives in **Detroit, Michigan, US**. This leadership position is crucial for driving innovation and advancing our client's scientific endeavors. You will be responsible for guiding a team of researchers in conceptualizing, designing, and executing sophisticated research projects. Your expertise will be vital in developing new methodologies, analyzing complex data sets, and interpreting results to inform future research directions. The Senior Research Lead will manage project timelines, budgets, and resources effectively, ensuring that research goals are met efficiently and within established parameters. Key responsibilities include staying abreast of the latest scientific advancements and publications in relevant fields, and identifying opportunities for novel research applications. You will contribute to the development of grant proposals and secure funding for research projects. Collaboration with internal departments, external academic institutions, and industry partners is essential for fostering a robust research ecosystem. The ideal candidate will possess a Ph.D. in a relevant scientific discipline such as Biology, Chemistry, Physics, Engineering, or a related field, along with a minimum of 7 years of post-doctoral research experience. Demonstrated leadership experience, a strong publication record in peer-reviewed journals, and a proven ability to secure research funding are required. Exceptional analytical, critical thinking, and problem-solving skills are paramount. Excellent communication, presentation, and interpersonal skills are necessary to effectively lead a team and disseminate research findings to diverse audiences. This is an unparalleled opportunity to contribute to significant scientific discoveries and shape the future of research within our organization.

Lumanity Medical Communications

Lumanity is dedicated to improving patient health by accelerating and optimizing access to medical advances. We partner with life sciences companies around the world to generate evidence to demonstrate the value of their product, translate the science and data into compelling product narratives, and enable commercial decisions that position these products for success in the market. We do this through strategic and complimentary areas of focus: Strategy & Insights, Value, Access & Outcomes, and Medical Strategy & Communications.

Position Overview

We are seeking an advanced degree life sciences professional to join our Medical Communications team and serve as the Scientific Director/Associate Scientific Director. This position falls within our wider Medical Strategy and Communications practice. We focus on strengthening the bridge between clinical and commercial, drawing from our foundation of scientific knowledge, regulatory expertise, and industry experience.

The Scientific Director/Associate Scientific Director will oversee the development of technically accurate and high-quality deliverables for Publications/Medical Affairs accounts. This role will serve as a strategic partner to clients and ensure projects and deliverables are on time and within budget. The Scientific Director/Associate Scientific Director will also direct the editorial component of projects, lead a team of medical writers, and ensure the accuracy, quality, and content of all written material.

Qualifications

The ideal candidate will have:

• PhD, PharmD, or MD required
• Minimum of 4-5+ years' medical writing experience in an agency or pharmaceutical company setting
• CMPP preferred, but not required

Benefits

We offer our employees a comprehensive benefits package that focuses on what matters to you health and well-being, personal finances, professional development, and a healthy work/life balance:

• Competitive salary plus bonus scheme
• Medical, dental, and vision insurance options
• 401(k) plan with employer match
• Flexible paid time off program + 10 paid holidays
• Flexible spending accounts for health and dependent care
• Health savings account option with employer contribution
• Employee Assistance Program
• Paid short-term and long-term disability coverage
• Company-paid life insurance coverage at 1.5x annual salary
• Paid parental leave and more

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about.
**Job Summary**
Serve as a scientist in the conduct of assigned nonclinical research studies of basic to moderate complexity, to include study management, interpretation and reporting of study data, and assuring the regulatory compliance of these projects.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
* Serve as a study director in the direction and execution of assigned studies in compliance with GLP regulations as they apply to the conduct of nonclinical research.
* Participate in proposal management and bid development process. Assist in the review of Letters of Commitment (LOC) in cooperation with client services.
* Participate in and coordinate all phases of the study planning process with appropriate departments.
* Generate high-quality protocols, amendments, and reports appropriate for assigned studies.
* Review, interpret, integrate, and present data on assigned studies, using the assistance of senior scientific staff as appropriate.
* Function as contact for the planning and execution of sponsor interaction related to assigned studies, including proposal management and study scheduling, conduct and reporting.
* Provide technical and scientific guidance to the research staff.
* Attend scientific meetings, conferences, and training courses to enhance job and professional skills.
* Perform all other related duties as assigned.
The pay range for this position is between $87,000 to $93,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
**Job Qualifications**
Education: Ph.D. or equivalent in toxicology or related scientific related discipline.
* Experience: 0 - 1 year.
* An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
* Certification/Licensure: N/A.
* Other: Understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs and the Good Laboratory Practices (GLPs), as appropriate. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in the use of standard software including Microsoft® Excel, Word, PowerPoint, etc. and with standard laboratory calculations.
PHYSICAL DEMANDS:
* While performing the duties of this job, the employee is regularly required to talk, hear and work/ type at a computer.
* Specific vision abilities required by this job include close vision and the ability to adjust focus.
WORK ENVIRONMENT:
* General office working conditions, the noise level in the work environment is usually quiet. Regularly enters vivarium laboratory areas, with proper utilization of protective laboratory.
* While performing the duties of this job the employee may occasionally be required to wear protective clothing (goggles, face shield, surgical mask, cap, gloves, scrubs, boots), work near toxic or caustic chemicals, work with biohazards, and/or work with live animals with risk of exposure to allergens and/or zoonotic diseases.
* The employee may occasionally be exposed to fumes or airborne particles, unpleasant odors, and/or wet, humid and/or extreme temperature conditions.
**About Safety Assessment**
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.
**About Charles River**
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.
We're committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.
**Equal Employment Opportunity**
Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.
It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit

Our client is a leading research and development firm seeking a highly accomplished Principal Scientific Research Scientist specializing in Materials Science to join their advanced research team in Grand Rapids, Michigan, US . This senior role will lead groundbreaking research initiatives, driving innovation in the development of novel materials and advanced manufacturing processes. The ideal candidate will possess a deep theoretical understanding and extensive practical experience in materials characterization, synthesis, and performance evaluation, with a focus on emerging applications. You will be responsible for conceptualizing and executing complex research projects, mentoring junior scientists, and collaborating with cross-functional teams to bring new materials from concept to commercialization. Key responsibilities include designing and conducting advanced experiments, analyzing experimental data using sophisticated techniques, publishing research findings in peer-reviewed journals, and presenting work at international conferences. You will also be instrumental in securing research funding through grant writing and identifying new research avenues. Expertise in areas such as nanotechnology, polymers, composites, or advanced metallurgy is highly desirable. A strong track record of innovation, problem-solving, and leadership within a scientific research environment is essential. The ability to manage research projects, budgets, and timelines effectively, while ensuring adherence to safety and quality standards, is critical. This is a premier opportunity to contribute significantly to the frontiers of materials science in Grand Rapids .

Qualifications:

• Ph.D. in Materials Science, Chemistry, Physics, Chemical Engineering, or a closely related scientific discipline.
• Minimum of 10 years of post-doctoral research experience in materials science or a related field, with significant experience in a lead or principal investigator role.
• Demonstrated expertise in materials synthesis, characterization techniques (e.g., SEM, TEM, XRD, spectroscopy), and performance testing.
• Proven track record of independent research, innovation, and publication in high-impact scientific journals.
• Experience with computational materials science and modeling is a plus.
• Strong project management skills and experience managing research grants and budgets.
• Excellent leadership, mentoring, and team collaboration skills.
• Exceptional analytical, problem-solving, and critical-thinking abilities.
• Strong written and verbal communication skills, with the ability to present complex scientific information effectively.
• Experience with intellectual property development and patent applications.

Join our world-class research team in Grand Rapids and lead the charge in materials innovation.

Scientific Director Medical Affairs & Publications

Come join an organization where growth is limitless even when joining at the director level. This is a standout opportunity to step into a high-impact role one a well-established account within a dynamic and innovative therapeutic area. We're actively seeking candidates based on the East Coast. Searching for candidates who are motivated to make the move to a new, amazing opportunity.

About the Role:

We are seeking a dynamic and strategicScientific Director to lead scientific content development across bothMedical Affairs andPublications initiatives. In this hybrid role, you will play a pivotal part in shaping scientific strategy, ensuring accuracy and alignment across deliverables, and serving as a key scientific partner to clients and internal teams.

Key Responsibilities:

Publications (approx. 40%)

• Lead the development and execution of comprehensive publication plans
• Provide strategic guidance and scientific direction on manuscripts, abstracts, posters, and congress presentations
• Collaborate with key opinion leaders (KOLs), authors, and clients to ensure high-quality, timely deliverables
• Ensure adherence to GPP and ICMJE guidelines and client SOPs
• Oversee internal and external medical writing resources and quality control

Medical Affairs (approx. 60%)

• Develop and deliver high-impact scientific content for advisory boards, symposia, and internal training initiatives
• Partner with cross-functional teams to translate complex science into compelling narratives for multiple stakeholders
• Support strategic planning and insight generation through literature reviews, gap analyses, and competitive intelligence
• Contribute to the development of medical platforms, scientific lexicons, and core messaging documents

Qualifications:

• Advanced degree (PhD, PharmD, MD, or equivalent) in life sciences required
• Minimum 5-7 years experience in a medical communications or agency setting
• Proven track record in both publications and medical affairs deliverables
• Deep understanding of therapeutic landscapes and scientific trends
• Excellent communication, leadership, and client-facing skills
• Ability to manage multiple projects and mentor junior team members

Why Join Us?

• Collaborate with a passionate and seasoned team of medical communicators
• Opportunity to shape strategy and drive scientific excellence across high-visibility projects

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Scientific Director

Citrus Health Group is a unique partner to the pharmaceutical, biotechnology, diagnostics, and medical device industries. We are passionate about science; our focus is to effectively communicate science in compelling and engaging ways to drive true value and enable patients to gain access to new medicines. We do so with the highest level of integrity and respect for the ethical nature of our business.

We invite you to join our talented team of dedicated professionals, working together to deliver the highest level of strategic advice, client service, and scientific, medical, real-world content to our clients. We are driven by one word, RESPECT. We respect each other, we respect our clients, and we respect the professionals we work with on behalf of our clients. We value every team member and strive for an inclusive and collaborative culture that fosters the best in everyone.

About the Opportunity

The CiTRUS Scientific Director has responsibility for providing scientific direction, leadership, and oversight over all projects on their accounts. The Scientific Director will seek out, examine, and distill complex scientific data to create impactful scientific publications, effective educational materials, and/or innovative brand strategies as needed by their client(s). They will understand the scientific and clinical aspects of assigned client work and serve as a key, strategic thought partner for both clients and internal teams. The Scientific Director is hallmarked by scientific and technical excellence within their accounts, as a source of therapeutic expertise within the Company, and as a provider of strategic scientific counsel internally and externally.

Job Description

The Scientific Director provides strategic scientific and publications oversight across multiple accounts. The key responsibilities are as follows: 1) review all content for scientific accuracy and adherence to client preference (e.g., lexicon, scientific communication platform); 2) provide ongoing training and feedback to internal team members; and 3) develop de novo content as needed (e.g., abstracts, posters, manuscripts, slide decks). The Scientific Director will identify emerging trends within applicable scientific areas and keep teams apprised. Leveraging strong scientific and creative expertise, they will guide and drive the strategic development of CiTRUS to provide scientific counsel both internally and to their clients and will provide support in identifying and converting new opportunities.

Scientific Account Services

• Lead all activities related to scientific strategies and publication planning, including oversight of scientifically complex materials
• Serve as a subject matter expert on scientific and clinical aspects of client projects and deliverables
• Support ongoing training of team members
• Continuously offer strategic and innovative ideas to support in achieving client and team objectives
• Support cross-functional teams to meet client needs
• Review deliverables with a scientific lens to ensure quality standards and ensure client expectations are met
• Ensure timely delivery of high-quality products and services to clients
• Keep leadership informed of critical client and project updates and concerns
• Keep abreast of the scientific developments relevant to accounts, disseminating information to the broader account team in a regular and timely manner, and to clients as appropriate

Client Management

• Prepare strategic and tactical plans for each client and individual project plans as needed
• Attend and lead aspects of regular client status meetings, new project kick-offs, and debrief meetings; communicate key learnings to client and internal team
• Regularly review project reports and alert client and project teams of emerging trends and any shifting clinical data points
• Expedite development of CiTRUS' scientific reputation with each client
• Ensure a high level of service, mutual respect and trust to create effective partnerships with clients, key experts, and other external partners
• Liaise effectively with clients and key experts, acting as the primary point of contact according to account requirements

External Communications

Where appropriate and necessary, communicate with authors and/or clients concerning project status and changes

• Actively participate in client presentations, communicating and promoting CiTRUS' expertise and informed perspectives
• Support project team in proactively anticipating, addressing, and responding to author/client requests
• Support the development of New Business, working with the commercial team as appropriate to identify and convert new targets and opportunities
• Provide scientific support in the development of proposals/pitches as appropriate

Qualifications

Education

Higher degree in the life sciences; PhD, MD or PharmD preferred

Experience

• 6+ years of publications experience within the pharmaceutical or medical communications industry
• Demonstrated understanding of product life cycles, competitive landscapes, and role of publications in client's medical and commercial strategies
• Experience translating complex data into effective presentation formats

Special Knowledge / Skills

• Strong understanding of clinical research and analyses
• Strong attention to detail and accuracy
• Ability to identify key issues; creatively and strategically overcome challenges
• High level of integrity, confidentiality, and accountability
• Ability to think analytically and to effectively plan, prioritize, and execute
• Expert verbal and written communication skills
• Expert presentation skills with a variety of formats to a variety of audiences
• Ability to work to the allocated deadlines and specification
• Understanding and application of good publications and practice and relevant compliance requirements
• Proficiency in Microsoft Suite; especially Microsoft PowerPoint, with the ability to produce well-designed and effective decks

Additional Information

Citrus Health Group is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service, or any other class protected by state or federal law.

Who we are

Healthcare Consultancy Group (HCG) is the global healthcare communications partner for pharma and biotech that accelerates the impact of medical science.

HCG boldly defines the healthcare communications landscape at the convergence of people, purpose, science and technology, driving the impact that pharma needs to realize the promise of innovative medicines.

We've created a unique model of four powerhouses- Commercial & Marketing, Medical Affairs, Publications, Regulatory - that enables hyperconnected, audience-centric engagement that delivers health impacts for our clients.

Why? Science requires it. HCP's demand it. Patients deserve it. Pharma inspires it.

Our Purpose

We accelerate the impact of science.

Scientific discovery moves humanity forward, creating better ways to connect, to care, to live. The innovations our clients create not only improve lives but save them. We work every day to maximize that impact.

With the unrivaled ability to define what's next, we keep clients ahead of the evolving industry landscape. Equal experts in the science and the humans behind it, we interrogate our client's challenge to identify real opportunity. Our industry foresight is matched with relentless execution, and we partner with clients to ensure their story connects with the right audience when it matters most.

Together, we move medicine closer to patients. Together, we accelerate the impact of science.

Scientific Associate

WHAT DOES A SCIENTIFIC ASSOCIATE DO?

Principal responsibilities include scientific content development based on relevant literature analysis, fact-checking, and participation in internal and external meetings in support of our pharmaceutical, biotech, and medical device clients. In this role, you will perform literature searches and evaluation to support development of various types of innovative deliverables, including their formatting, referencing, and annotation. In each project, you will have the opportunity to monitor and manage budget and timelines, while preserving high quality and accuracy standards. As the key member of the scientific team, you will engage and collaborate with clients and contribute to the overall team success.

QUALIFICATIONS

• PhD, PharmD or MD in biomedical sciences
• Experience with critical evaluation of scientific/medical publications
• Experience developing slide decks and manuscripts based on available evidence
• PowerPoint, Word, Excel, Microsoft Outlook, and Internet research proficiency
• Exceptional written and oral communication skills
• Strong attention to detail and organizational skills
• Demonstrated ability to perform effectively in a collaborative team structure and thrive in a fast-paced environment.

WHAT WE OFFER:

• A competitive compensation package
• Paid annual vacation, holiday and sick time off
• Comprehensive health plans including medical, dental and vision
• Competitive 401(k) investment options
• Employee stock purchase plan
• Life insurance
• Commuter benefits
• Employee referral awards
• Employee Assistance Program
• Tuition reimbursement
• Training and mentoring opportunities through programs such as Omnicom University, led by international influencers and Harvard Business School professors
• Retail and entertainment discounts and benefits available
• A rewarding workplace and a fun team environment

The salary range for this position is $70,000 to $5,000 . This range represents the low and high end of the salary someone in this role may earn as an employee of an HCG Agency in the United States. Salaries will vary based on various factors, including but not limited to, professional and academic experience, training, responsibilities of the position, and other business and organizational needs. The range listed is just one component of our total compensation package for employees. Salary decisions are dependent on the circumstances of each hire. HCG reserves the right to modify this pay range at any time If your requirements fall outside of this range, you are still welcome to apply.

Healthcare Consultancy Group is an Equal Opportunity Employer. All applicants will be considered without regard to race, color, religion, sex, age, national origin, citizenship status, sexual orientation, disability, veteran status or any category or class of person protected by law.

US Salary Range

70,000- 85,000 USD

Omnicom Health is committed to hiring and developing exceptional talent. We agree that talent is uniquely distributed, and we're focused on developing inclusive teams that can bring the best solutions to everything we do. We strongly believe that celebrating what makes us different makes us better together. Join us-we look forward to getting to know you. We will process your personal data in accordance with our Recruitment Privacy Notice.