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Clinical Science Manager Jobs in Georgia (NOW HIRING)

The Sr. Manager, Medical Field integrates clinical/scientific expertise and knowledge to ensure successful implementation of the medical affairs strategic plan within an assigned geographic region.

The Sr. Manager, Medical Field integrates clinical/scientific expertise and knowledge to ensure successful implementation of the medical affairs strategic plan within an assigned geographic region.

Bachelor's or Master's degree in Life Sciences, Data Science, Computer Science, or a related field. * 7+ years of clinical data management experience, with at least 2 years in a senior or lead role.

Bachelor's or Master's degree in Life Sciences, Data Science, Computer Science, or a related field. * 7+ years of clinical data management experience, with at least 2 years in a senior or lead role.

Sr Manager Clinical Relations

Stockbridge, GA · On-site

$55K - $76K/yr

The College of Nursing offers a three-year Bachelor of Science in Nursing degree program and ... Manage implementation of clinical operations at all new campuses and new BSN online hub markets.

Sr Manager Clinical Relations

Atlanta, GA · On-site

$62K - $86K/yr

The College of Nursing offers a three-year Bachelor of Science in Nursing degree program and ... Manage implementation of clinical operations at all new campuses and new BSN online hub markets.

Clinical Research Manager

Atlanta, GA · On-site

$85 - $125/hr

Bachelor's degree in nursing, life sciences, public health, healthcare administration, or a related ... clinical research experience, including study coordination or site management and direct ...

Ability to quickly understand and translate complex scientific data and realize its potential impact on clinical practice and research needs. * Experience in managed care/PBM, HEOR activities, or ...

Showing results 21-40

Clinical Science Manager information

See Georgia salary details

$36.7K

$69.5K

$118.2K

How much do clinical science manager jobs pay per year?

As of Sep 7, 2026, the average yearly pay for clinical science manager in Georgia is $69,535.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,900.00 and $75,600.00 per year, depending on experience, location, and employer.

What is a clinical science manager?

Clinical Science Managers are professionals who oversee and coordinate clinical research projects, often within the pharmaceutical, biotechnology, or medical device industries. They are responsible for managing clinical trials, ensuring regulatory compliance, and collaborating with cross-functional teams such as clinical operations, regulatory affairs, and medical affairs. Their role involves protocol development, data analysis, and ensuring the safety and efficacy of investigational products. Clinical Science Managers also play a critical part in interpreting study results and presenting findings to stakeholders. They typically have advanced degrees in life sciences and significant experience in clinical research.

What are the key skills and qualifications needed to thrive as a clinical science manager?

To thrive as a Clinical Science Manager, you need a solid background in clinical research, life sciences, and project management, typically supported by an advanced degree (e.g., PharmD, PhD, or MD) and industry experience. Familiarity with clinical trial management systems, regulatory compliance tools, and data analysis platforms is crucial. Strong leadership, strategic thinking, and effective communication skills help you manage cross-functional teams and build relationships with stakeholders. These competencies ensure the successful design, execution, and oversight of clinical studies, ultimately advancing scientific and business goals.

How does a clinical science manager typically collaborate with cross-functional teams during clinical trial development?

Clinical Science Managers play a key role in bridging scientific objectives with operational execution by working closely with clinical operations, regulatory affairs, data management, and medical affairs teams. They often lead the development of clinical protocols and ensure scientific integrity throughout the study, facilitating regular meetings and communication to align project goals and timelines. Their collaborative efforts help anticipate and resolve challenges, streamline processes, and ensure that trials meet regulatory requirements and scientific standards.

What is the difference between Clinical Science Manager vs Clinical Research Associate?

AspectClinical Science ManagerClinical Research Associate
CredentialsTypically requires advanced degrees (e.g., Master’s or PhD) and industry experienceUsually holds a bachelor’s degree in life sciences or related field
Work EnvironmentLeads teams, manages projects, and oversees clinical studiesMonitors clinical trials at sites, ensures protocol compliance
Employer & Industry UsagePharmaceutical, biotech, and medical device companiesContract research organizations, pharmaceutical companies
Search & Comparison IntentUnderstanding managerial roles in clinical scienceFocus on trial monitoring and site management

The Clinical Science Manager typically oversees clinical projects and manages teams, requiring advanced credentials. In contrast, the Clinical Research Associate focuses on monitoring clinical trials at sites. Both roles are essential in the clinical research process but differ in responsibilities and experience levels.

What cities in Georgia are hiring for Clinical Science Manager jobs?

Cities in Georgia with the most Clinical Science Manager job openings:

Infographic showing various Clinical Science Manager job openings in Georgia as of August 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $69,535 per year, or $33.4 per hour.

Sr. Manager, Medical Field

Taiho Oncology, Inc.

Atlanta, GA • On-site

Full-time

Retirement, PTO

Re-posted 17 days ago


Job description

Looking for a chance to make a meaningful difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers. Our "People first" approach means we also highly value our employees, who work relentlessly to help execute our mission. Taiho's success is founded on ensuring we always act with accountability, collaboration, and trust. By following these guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other. Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower us to innovate and touch the lives of more and more patients. It's our work, our passion, and our legacy. We invite you to join us.
Field
The preferred candidate will reside in NC, SC, GA, TN or KY, and near a major airport hub such has Atlanta, Nashville, Raleigh, Charlotte or similar location.
Employee Value Proposition:
Exciting opportunity to join a medical field team and collaborate with a dynamic and growing Medical Affairs Department.
Position Summary:
The Sr. Manager, Medical Field is a field-facing representative of the Medical Affairs Department with a primary responsibility to engage in the exchange of scientific data, education of health care practitioners on Taiho products and relevant disease states, and facilitation of clinical research. The Sr. Manager, Medical Field integrates clinical/scientific expertise and knowledge to ensure successful implementation of the medical affairs strategic plan within an assigned geographic region. The Sr. Manager, Medical Field brings relevant insights from the field on research developments, treatment landscape and new concepts in medical treatment. The role of the Sr. Manager, Medical Field is non-promotional in nature.
Performance Objectives:
Product/Therapeutic Area Support to External Stakeholders:
  • Act as the primary clinical/scientific resource to HCPs in a specified geography for information pertaining to disease state and Taiho's product(s) and compounds to ensure awareness and understanding.
  • Provide high quality scientific information to healthcare professionals (HCPs).
  • Serve as a conduit for accurate and updated clinical, scientific, and medical information between Key Opinion Leaders (KOLs)/investigators and the company's Medical Affairs and development groups.
  • Establish, foster, cultivate, and maintain peer relationships with KOLs and HCPs in the therapeutic areas in which Taiho has current and future interests.
  • Share knowledge and participate in scientific exchanges and interactions with identified KOLs.
  • Present clinical and scientific data on Taiho's products and relevant therapeutic areas as requested.
  • Identify and report key scientific, clinical and research insights from KOLs and HCPs to Medical Affairs.
  • Respond to unsolicited medical information requests in the field.
  • Fulfill Pharmacovigilance responsibilities as defined in the pharmacovigilance SOPs related to medical inquiries and drug safety information.
  • Use medical affairs plans to develop and align the tactical plan for Sr. Manager Medical Field geography of responsibility and implement plans to support Medical Affairs strategic direction for assigned territory, e.g., medical territory plan.

Training/Education Resource:
  • Develop, maintain, and demonstrate scientific expertise and a strong knowledge of hematology-oncology, disease states which are of interest to Taiho Oncology, study methodology, GCP, clinical information, and product data.
  • Demonstrate full knowledge of and ability to execute on approved medical platforms/strategies and initiatives.
  • Serve as technical/scientific subject matter resource to Taiho commercial personnel, if requested.

Research Support:
  • At the local level, identify opportunities for collaboration in Real World Evidence with internal Medical Affairs personnel.
  • In collaboration with Medical Affairs personnel support data generation Investigator-Initiated Trials (IITs) and HCP initiated projects.
  • Facilitate the review and follow-up of submitted IITs.
  • Assist with Taiho sponsored trials as assigned, which may include providing recommendations for site selection, clinical data presentation at site initiation or training meetings, and communication of scientific insights for specific studies from clinical sites to internal TOI departments.

Professional Organization Support:
  • Work in conjunction with the appropriate internal departments to support Taiho's collaboration and interactions with professional organizations/societies & advocacy groups, GPOs, and large networked practices.
  • Collaborate with internal colleagues and KOLs/HCPs on Medical Affairs initiatives including publications as requested, advisory boards, medical meeting support, medical education opportunities, training, speaker development, etc.

Education/Certification Requirements:
  • A terminal D degree (i.e., MD, PharmD or PhD) in medical or health sciences is strongly preferred or equivalent.

Knowledge, Skills, and Abilities:
  • Three years of experience in a field facing scientific role is preferred and Medical Field experience is preferred.
  • Experience in the pharmaceutical industry is preferred.
  • One or more years of oncology experience is preferred.
  • Knowledge of oncology KOLs, HCPs, and institutions in the geography to be covered is preferred.
  • Knowledge of clinical trials is preferred.
  • Knowledge of treatment guidelines, clinical research processes, FDA regulations and OIG guidelines are required.
  • Excellent interpersonal communication and presentation skills are required.
  • Ability to network and partner with important external customers, including medical thought leaders, academic institutions, large group practices, medical directors and pharmacy directors is required.
  • Demonstrated ability and experience working cross-functionally, as well as influencing and negotiating at all levels within the organization.
  • Demonstrated ability to anticipate, organize, plan and handle multiple changing priorities.
  • Demonstrated ability to work independently while adhering to Medical Affairs strategic direction.
  • Demonstrated proficiency in communicating upward, downward, and laterally, verbally and in writing.
  • Demonstrated ability to analyze complex situations and proactively identify opportunities/issues; effectively solve problems that cross functional boundaries.
  • Committed to the concept of team and working within the framework of the Medical Affairs Department and Taiho organization, including as it pertains to compliance with policies, systems and practices.
  • Possesses and maintains a valid driver's license.
  • Ability to read, analyze and interpret scientific and technical information and data.
  • Excellent English communication skills, both verbal and written.
  • Individual should be able to apply critical thinking process in order to optimize strategic initiatives and decision making.
  • Requires operational proficiency with power point, word and excel.
  • Demonstrated ability to work with software tracking/logging systems.

The pay range for this position at commencement of employment is expected to be between $178,500 - $210,000 annually. This pay range is based on the market range for positions of this type. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including annual bonus/incentive comp plans, potential long term incentive plan, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if a candidate/employee receives an offer of employment.
If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
#Atlanta, Georgia-United States
Equal Opportunity Employer Information: Taiho Oncology is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, gender, sex, age, religion, creed, national origin, ancestry, citizenship, marital status, sexual orientation, physical or mental disability, medical condition, veteran status, gender identity, genetic information, or any other characteristic protected by federal, state, or local law. Any applicant who, because of a disability, needs an accommodation or assistance in completing an application or at any time during the application process, please email People@taihooncology.com. Taiho Oncology also provides reasonable accommodations to employees with disabilities consistent with our obligations under the law. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment qualified applicants with arrest and conviction records.
The incumbent in this position may be required to perform other duties, as assigned.