Senior Researcher Jobs at Syneos Health with Visa Sponsorship
Senior Researcher jobs at Syneos Health sit at the intersection of clinical science and drug development, requiring deep expertise in study design, data analysis, and regulatory standards. Syneos Health has an established track record of sponsoring international researchers across multiple visa categories, making it a real option for qualified candidates who need work authorization.
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Get Access To All JobsINTRODUCTION
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
* Please note, this position is heavily focused on operational and project coordination support within RWE and Late Phase research environments. We are specifically seeking candidates who already have exposure to Real World Evidence programs, epidemiology, observational or outcomes research, and/or Clinical Data Management support within Pharmaceutical, Biotechnology, or CRO organizations. Candidates without this experience will not be considered. Thank you! *
Senior Project Specialist – Real World Evidence (Sponsor Dedicated /Remote -US Based)
Are you looking to grow your career in one of the fastest-evolving areas of clinical research and healthcare analytics?
We are seeking a Senior Project Specialist – Real World Evidence (RWE) to join a sponsor-dedicated team supporting innovative pharmaceutical research programs focused on real-world data and evidence generation. This role is ideal for someone who enjoys organization, coordination, problem-solving, and working behind the scenes to help complex research programs run smoothly.
While this is an administrative and operational support-focused position, it is important that candidates already have exposure to the Real World Evidence (RWE) space and understand the fundamentals of how RWE studies and teams operate.
This could be a great fit for someone who has supported:
- Real World Evidence (RWE) teams
- Epidemiology or observational research programs
- Outcomes research initiatives
- Data Management teams within Pharmaceutical, Biotechnology, or CRO environments
and is looking to continue building their career in this exciting and growing specialty area.
What You’ll Be Doing
In this role, you will support project teams responsible for both:
- Secondary data studies
- Primary data collection studies
You’ll work closely with Project Leads, epidemiologists, data analysts, Data Management teams, and cross-functional stakeholders to help keep projects organized, on track, and moving forward.
Your day-to-day work may include:
- Coordinating and updating study milestones and timelines
- Supporting project tracking within CTMS systems
- Scheduling and coordinating meetings
- Preparing meeting minutes and follow-up action items
- Helping teams stay organized across multiple deliverables
- Supporting operational activities for ongoing RWE studies
- Assisting with documentation, reporting, and project coordination
- Helping facilitate communication between study teams, analysts, and stakeholders
This is a highly collaborative role where organization, communication, and attention to detail are key.
What We’re Looking For
Required
- Prior experience supporting work within:
- Real World Evidence (RWE)
- Clinical Data Management
- Epidemiology
- Observational or outcomes research environments
- Experience within a Pharmaceutical, Biotechnology, or CRO setting
- Understanding of:
- Secondary data research
- Primary data collection studies
- CTMS systems and/or clinical research operations
- Strong organizational and coordination skills
- Ability to manage multiple tasks and deadlines in a fast-paced environment
- Strong communication and interpersonal skills
- Proficiency with Microsoft Office applications
- Experience with Late Phase and RWE projects supporting regulatory purposes, including pivotal or supportive evidence generation, is considered a strong asset
Nice to Have (But Not Required)
- Experience working directly with epidemiology or data analytics teams
- Sponsor-dedicated or embedded team experience
- Exposure to healthcare databases or real-world data sources
- Life sciences or healthcare-related degree
- Interest in long-term growth within RWE, clinical operations, or healthcare analytics
Why This Role Stands Out
Real World Evidence is transforming how therapies are studied, understood, and brought to patients. This role offers the opportunity to gain hands-on experience supporting high-impact research programs while working alongside experienced professionals across clinical operations, epidemiology, data management, and analytics.
If you are someone who enjoys keeping projects organized, supporting collaborative teams, and being part of meaningful healthcare research, we would love to hear from you!
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:
$47,000.00 - $79,900.00
The 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.
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.
INTRODUCTION
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
* Please note, this position is heavily focused on operational and project coordination support within RWE and Late Phase research environments. We are specifically seeking candidates who already have exposure to Real World Evidence programs, epidemiology, observational or outcomes research, and/or Clinical Data Management support within Pharmaceutical, Biotechnology, or CRO organizations. Candidates without this experience will not be considered. Thank you! *
Senior Project Specialist – Real World Evidence (Sponsor Dedicated /Remote -US Based)
Are you looking to grow your career in one of the fastest-evolving areas of clinical research and healthcare analytics?
We are seeking a Senior Project Specialist – Real World Evidence (RWE) to join a sponsor-dedicated team supporting innovative pharmaceutical research programs focused on real-world data and evidence generation. This role is ideal for someone who enjoys organization, coordination, problem-solving, and working behind the scenes to help complex research programs run smoothly.
While this is an administrative and operational support-focused position, it is important that candidates already have exposure to the Real World Evidence (RWE) space and understand the fundamentals of how RWE studies and teams operate.
This could be a great fit for someone who has supported:
- Real World Evidence (RWE) teams
- Epidemiology or observational research programs
- Outcomes research initiatives
- Data Management teams within Pharmaceutical, Biotechnology, or CRO environments
and is looking to continue building their career in this exciting and growing specialty area.
What You’ll Be Doing
In this role, you will support project teams responsible for both:
- Secondary data studies
- Primary data collection studies
You’ll work closely with Project Leads, epidemiologists, data analysts, Data Management teams, and cross-functional stakeholders to help keep projects organized, on track, and moving forward.
Your day-to-day work may include:
- Coordinating and updating study milestones and timelines
- Supporting project tracking within CTMS systems
- Scheduling and coordinating meetings
- Preparing meeting minutes and follow-up action items
- Helping teams stay organized across multiple deliverables
- Supporting operational activities for ongoing RWE studies
- Assisting with documentation, reporting, and project coordination
- Helping facilitate communication between study teams, analysts, and stakeholders
This is a highly collaborative role where organization, communication, and attention to detail are key.
What We’re Looking For
Required
- Prior experience supporting work within:
- Real World Evidence (RWE)
- Clinical Data Management
- Epidemiology
- Observational or outcomes research environments
- Experience within a Pharmaceutical, Biotechnology, or CRO setting
- Understanding of:
- Secondary data research
- Primary data collection studies
- CTMS systems and/or clinical research operations
- Strong organizational and coordination skills
- Ability to manage multiple tasks and deadlines in a fast-paced environment
- Strong communication and interpersonal skills
- Proficiency with Microsoft Office applications
- Experience with Late Phase and RWE projects supporting regulatory purposes, including pivotal or supportive evidence generation, is considered a strong asset
Nice to Have (But Not Required)
- Experience working directly with epidemiology or data analytics teams
- Sponsor-dedicated or embedded team experience
- Exposure to healthcare databases or real-world data sources
- Life sciences or healthcare-related degree
- Interest in long-term growth within RWE, clinical operations, or healthcare analytics
Why This Role Stands Out
Real World Evidence is transforming how therapies are studied, understood, and brought to patients. This role offers the opportunity to gain hands-on experience supporting high-impact research programs while working alongside experienced professionals across clinical operations, epidemiology, data management, and analytics.
If you are someone who enjoys keeping projects organized, supporting collaborative teams, and being part of meaningful healthcare research, we would love to hear from you!
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:
$47,000.00 - $79,900.00
The 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.
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.
See all Senior Researcher Jobs at Syneos Health
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Senior Researcher Jobs at Syneos Health.
Get Access To All JobsTips for Finding Senior Researcher Jobs at Syneos Health
Align your credentials to clinical research standards
Syneos Health Senior Researcher roles typically require a graduate degree in a life sciences field. If your degree was earned outside the U.S., get a credential evaluation from a NACES-approved evaluator before applying so your qualifications translate clearly to hiring managers.
Target therapeutic areas where Syneos hires repeatedly
Syneos Health runs ongoing research across oncology, cardiovascular, and CNS programs. Tailoring your resume and cover letter to a specific therapeutic area rather than applying broadly signals genuine fit and moves you past initial screening faster.
Search and filter verified sponsorship roles on Migrate Mate
Use Migrate Mate to filter Senior Researcher openings at Syneos Health by visa type, so you only apply to roles where sponsorship is confirmed. This saves weeks of back-and-forth during early application stages.
Clarify TN eligibility before your first interview
If you hold Canadian or Mexican citizenship, TN classification can move faster than H-1B and avoids the lottery entirely. Confirm your degree and job title align with TN's approved Life Scientist or Scientific Technician categories before the offer stage.
Understand how H-1B cap timing affects your start date
If Syneos Health files an H-1B cap-subject petition for you, USCIS only accepts filings in April for an October 1 start. Build this into your negotiation so your expected start date and employment contract reflect the earliest possible work-authorized date.
Request written sponsorship commitment before signing
Before accepting a Senior Researcher offer, confirm in writing which visa category Syneos Health will file, whether they cover government filing fees, and whether they use premium processing. Vague verbal assurances can create problems once USCIS forms are being prepared.
Frequently Asked Questions
Does Syneos Health sponsor H-1B visas for Senior Researchers?
Yes, Syneos Health sponsors H-1B visas for Senior Researcher roles. As a contract research organization with ongoing clinical trial operations, the company regularly files H-1B petitions for research staff in specialty occupation roles. Cap-subject petitions are filed in April for an October 1 start, so your timeline and offer negotiations should account for that window.
Which visa types are commonly used for Senior Researcher roles at Syneos Health?
Senior Researchers at Syneos Health are sponsored under H-1B for most international candidates. F-1 OPT and STEM OPT extensions are also used for recent graduates, providing up to three years of work authorization before an H-1B petition is needed. TN visa classification is an option for Canadian and Mexican citizens in qualifying scientific roles. Green Card sponsorship through EB-2 or EB-3 is available for longer-tenured researchers.
What qualifications are expected for Senior Researcher roles at Syneos Health?
Syneos Health Senior Researcher positions generally require a master's or doctoral degree in a life sciences discipline such as pharmacology, biology, or clinical sciences. Hands-on experience with clinical trial protocols, biostatistics, or regulatory submission processes strengthens your application. Prior CRO or pharmaceutical industry experience is frequently preferred over academic research backgrounds alone.
How do I apply for Senior Researcher jobs at Syneos Health?
You can browse open Senior Researcher positions at Syneos Health directly through their careers portal or through Migrate Mate, which lets you filter by visa sponsorship type so you can confirm eligibility before applying. When applying, align your resume to the specific therapeutic area or research function listed in the job posting rather than submitting a generic application across multiple roles.
How do I manage my OPT timeline when targeting a Senior Researcher role at Syneos Health?
If you are on F-1 OPT, apply for your STEM OPT extension as early as possible since USCIS recommends filing at least 90 days before your initial OPT expires. A valid STEM OPT extension gives you up to 24 additional months of work authorization, which typically covers one full H-1B cap cycle. Syneos Health must be enrolled in E-Verify for your STEM OPT extension to be authorized.