Manager, Medical Operations
Raleigh, NC · On-site
Manager, Medical Operations ICON is a global healthcare intelligence and clinical research ... Minimum of five years of relevant experience in pharmaceutical, biotechnology, clinical research ...
Raleigh, NC · On-site
Manager, Medical Operations ICON is a global healthcare intelligence and clinical research ... Minimum of five years of relevant experience in pharmaceutical, biotechnology, clinical research ...
Raleigh, NC · On-site
Manager, Medical Operations ICON is a global healthcare intelligence and clinical research ... Minimum of five years of relevant experience in pharmaceutical, biotechnology, clinical research ...
Chapel Hill, NC · On-site
$200K - $250K/yr
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Chapel Hill, NC · On-site
$200K - $250K/yr
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Raleigh, NC · On-site
$200K - $250K/yr
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Raleigh, NC · On-site
$200K - $250K/yr
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Raleigh, NC · On-site
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Raleigh, NC · On-site
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Durham, NC · Remote
$154K - $431K/yr
Candidate should have a minimum 3 years clinical trials experience as a medical /clinical expert in the Pharma, CRO, or Biotech industry. * Experience in immunology clinical trials as Medical ...
Durham, NC · Remote
$154K - $431K/yr
Candidate should have a minimum 3 years clinical trials experience as a medical /clinical expert in the Pharma, CRO, or Biotech industry. * Experience in immunology clinical trials as Medical ...
Durham, NC · On-site
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Durham, NC · On-site
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Chapel Hill, NC · On-site
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Chapel Hill, NC · On-site
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Chapel Hill, NC · On-site
$200K - $250K/yr
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Chapel Hill, NC · On-site
$200K - $250K/yr
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Durham, NC · On-site
$200K - $250K/yr
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Durham, NC · On-site
$200K - $250K/yr
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Durham, NC · On-site
$200K - $250K/yr
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Durham, NC · On-site
$200K - $250K/yr
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Raleigh, NC · On-site
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Raleigh, NC · On-site
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Chapel Hill, NC · On-site
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Chapel Hill, NC · On-site
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Raleigh, NC · On-site
$200K - $250K/yr
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Raleigh, NC · On-site
$200K - $250K/yr
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Durham, NC · Remote
$154K - $431K/yr
Candidate should have a minimum 3 years clinical trials experience as a medical /clinical expert in the Pharma, CRO, or Biotech industry. * Experience in immunology clinical trials as Medical ...
Durham, NC · Remote
$154K - $431K/yr
Candidate should have a minimum 3 years clinical trials experience as a medical /clinical expert in the Pharma, CRO, or Biotech industry. * Experience in immunology clinical trials as Medical ...
Durham, NC · On-site
$154K - $431K/yr
Candidate should have a minimum 3 years clinical trials experience as a medical /clinical expert in the Pharma, CRO, or Biotech industry. * Experience in immunology clinical trials as Medical ...
Durham, NC · On-site
$154K - $431K/yr
Candidate should have a minimum 3 years clinical trials experience as a medical /clinical expert in the Pharma, CRO, or Biotech industry. * Experience in immunology clinical trials as Medical ...
Durham, NC · On-site
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Durham, NC · On-site
Act as the primary medical liaison for biotech partners, providing expert guidance on donor eligibility, product specifications, and clinical trial alignment. Provide medical oversight for the ...
Durham, NC · On-site
Minimum of 7 + years of experience in medical writing within the biopharmaceutical, biotechnology, or CRO industry; equivalent experience in clinical or preclinical development will also be ...
Durham, NC · On-site
Minimum of 7 + years of experience in medical writing within the biopharmaceutical, biotechnology, or CRO industry; equivalent experience in clinical or preclinical development will also be ...
PSC Biotech provides the life sciences with essential services to ensure that health care products ... Medical, Dental, and Vision - PSC pays 100% of all qualifying employee medical premiums and 50% for ...
PSC Biotech provides the life sciences with essential services to ensure that health care products ... Medical, Dental, and Vision - PSC pays 100% of all qualifying employee medical premiums and 50% for ...
Durham, NC · On-site
Minimum of 7 + years of experience in medical writing within the biopharmaceutical, biotechnology, or CRO industry; equivalent experience in clinical or preclinical development will also be ...
Durham, NC · On-site
Minimum of 7 + years of experience in medical writing within the biopharmaceutical, biotechnology, or CRO industry; equivalent experience in clinical or preclinical development will also be ...
Durham, NC · On-site
Minimum of 7 + years of experience in medical writing within the biopharmaceutical, biotechnology, or CRO industry; equivalent experience in clinical or preclinical development will also be ...
Durham, NC · On-site
Minimum of 7 + years of experience in medical writing within the biopharmaceutical, biotechnology, or CRO industry; equivalent experience in clinical or preclinical development will also be ...
$16.81 is the 25th percentile. Wages below this are outliers.
$12.85 - $28.68
100% of jobs
$28.68 - $44.50
0% of jobs
$44.50 - $60.33
0% of jobs
$60.33 - $76.16
0% of jobs
$76.16 - $91.98
0% of jobs
$91.98 - $107.81
0% of jobs
$107.81 - $123.63
0% of jobs
$123.63 - $139.46
0% of jobs
$139.46 - $155.29
0% of jobs
$155.29 - $171.11
0% of jobs
$171.11 - $186.94
0% of jobs
$12
$73
$186
A Medical Biotechnology job involves applying biological and technological advancements to develop medical treatments, diagnostic tools, and pharmaceuticals. Professionals in this field work in research labs, healthcare companies, or biotech firms to create innovative solutions for diseases and medical conditions. Their tasks may include genetic engineering, drug development, tissue engineering, and clinical trials. This role requires expertise in molecular biology, biochemistry, and bioinformatics to improve healthcare outcomes.
Professionals in Medical Biotechnology often engage in projects such as developing diagnostic assays, conducting genetic research, or designing new medical therapies. Daily tasks may include performing laboratory experiments, analyzing biological data, writing technical reports, and maintaining meticulous records to comply with regulatory guidelines. Collaboration is common, as you'll frequently work alongside scientists, clinicians, and regulatory specialists to move projects forward. This diversity of responsibilities offers ample learning opportunities and exposure to cutting-edge technologies, preparing you for career advancement in both the laboratory and broader biotechnology industry.
To thrive in Medical Biotechnology, a solid background in biology, chemistry, and laboratory techniques is usually needed, along with at least a bachelor's degree in biotechnology or a related field. Hands-on experience with PCR, cell culture, DNA sequencing, and familiarity with lab safety protocols and regulatory standards are highly valued. Critical thinking, problem-solving, and effective teamwork are important soft skills for navigating research challenges and collaborating within multidisciplinary teams. These capabilities enable professionals to innovate, maintain compliance, and contribute meaningful advances in medical diagnostics and therapeutics.
The most popular types of Medical Biotechnology jobs in Raleigh, NC are:
For Medical Biotechnology jobs in Raleigh, NC, the most frequently searched job titles are:
The top searched job categories for Medical Biotechnology jobs in Raleigh, NC are:
Cities near Raleigh, NC with the most Medical Biotechnology job openings:

Full-time
Medical, Dental, Vision, Life, Retirement
This job post has expired today. Applications are no longer accepted.
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
What You Will Do:
Serve as the primary contact for completing IIR study budget Fair Market Value (FMV) assessment
Review, evaluate, and negotiate IIR study budgets and line-item requests with study sites to ensure alignment with FMV guidelines and organizational standards.
Partner with IIR Project Managers to review budget requests, resolve outstanding questions, and provide timely feedback to study sites.
Maintain internal budget benchmarking data and recommend updates based on market trends, historical experience, and current rates.
Prepare and distribute quarterly reports and summaries of finalized IIR study budgets.
Develop site budget templates and negotiation parameters, or review and approve CRO-developed budget templates to ensure consistency and alignment with organizational standards.
Review and provide guidance on site budget escalation requests submitted by CROs.
Supports the operational management of the US Oncology Investigator-Initiated Research (IIR) program by partnering with cross-functional stakeholders across US Medical Affairs, Clinical Development, and Alliance organizations. Facilitates communication, coordinates meetings, and maintains documentation to ensure alignment and efficient execution of program activities.
Maintains IIR tracking tools and performance metrics to provide portfolio visibility and support risk management. Additionally, supports vendor oversight activities, delivers training on IIR systems and processes, and serves as a point of contact for user support and issue resolution.
Your Profile:
Bachelor's degree (B.A. or B.S.) required.
Minimum of five years of relevant experience in pharmaceutical, biotechnology, clinical research, or related industry.
Demonstrated experience in study budget evaluation, FMV assessment, and site budget negotiation.
Demonstrated project management experience supporting clinical or Medical Affairs research.
Advanced proficiency with Microsoft Office applications, project management tools, and document management systems.
Demonstrated success in building productive relationships with diverse internal and external stakeholders through strong communication, collaboration, and interpersonal skills.
Dependable self-starter with strong organizational skills and the ability to manage competing priorities and meet strict deadlines in a highly metrics-driven environment.
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.
Are you a current ICON Employee? Please click here to apply