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Ibm Clinical Development Jobs (NOW HIRING)

Integrated Resources INC

IBM TECHNICAL LEAD

Buffalo, NY · On-site

... CLINICAL NURSING Inc. 5000 - 2007- 2013 (7th Year) Direct: (732) 549 2660 Tel: (732) 549-2030 x 127 Fax: (732) 549-5549 Additional Information Mobile Application Development Experience with IBM ...

Integrated Resources INC

IBM MDM Data Modeler

Charlotte, NC · On-site

$53.50 - $69.25/hr

Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. IBM MDM Data ... development of logical and physical data models Extend and customize the IBM data model based on ...

Trinity Health

Clinical Assistant - ER

Davenport, IA · On-site

Visit MercyOne Careers to learn more about the benefits, culture, and career development ... Recognition includes IBM Watson top-15 health system, Leapfrog "A" safety grade, U.S. News top ...

Orlando Health

Clinical Pharmacist

Orlando, FL · On-site

$110K - $132K/yr

S. News & World Report and was included, together with Orlando Health ORMC, in the IBM Watson ... and development over the life span and possesses the ability to assess data reflective of the ...

Orlando Health

Clinical Pharmacist

Orlando, FL · On-site

$110K - $132K/yr

S. News & World Report and was included, together with Orlando Health ORMC, in the IBM Watson ... and development over the life span and possesses the ability to assess data reflective of the ...

Orlando Health

Clinical Pharmacist

Orlando, FL · On-site

$110K - $132K/yr

S. News & World Report and was included, together with Orlando Health ORMC, in the IBM Watson ... and development over the life span and possesses the ability to assess data reflective of the ...

Orlando Health

Clinical Pharmacist

Orlando, FL · On-site

$110K - $132K/yr

S. News & World Report and was included, together with Orlando Health ORMC, in the IBM Watson ... and development over the life span and possesses the ability to assess data reflective of the ...

Integrated Resources INC

IIB Developer

Cincinnati, OH · On-site

Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Header: IIB ... IBM WebSphere Message broker and IBM MQ Series Experience in System Integration, Technical ...

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All JobsIbm Clinical Development Jobs

Ibm Clinical Development information

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$79.5K

$142.1K

$178.5K

How much do ibm clinical development jobs pay per year?

As of Jun 15, 2026, the average yearly pay for ibm clinical development in the United States is $142,102.00, according to ZipRecruiter salary data. Most workers in this role earn between $123,500.00 and $163,000.00 per year, depending on experience, location, and employer.

What do you do in clinical development?

In clinical development, professionals design, oversee, and monitor clinical trials to evaluate the safety and effectiveness of new medical treatments or drugs. They coordinate with research teams, ensure compliance with regulatory standards, and analyze data to support product approval processes.

How much does a clinical trial assistant earn?

A clinical trial assistant typically earns between $40,000 and $60,000 annually, depending on experience, location, and the organization. Entry-level positions may start lower, while experienced assistants with certifications can earn higher salaries. The role often requires familiarity with clinical trial protocols and data management tools.

What is IBM clinical development?

IBM Clinical Development is a cloud-based platform used in clinical research to manage and streamline data collection, monitoring, and analysis. Professionals working in this role typically handle electronic data capture (EDC), ensure compliance with regulatory standards, and utilize tools like Medidata or Oracle Clinical to support clinical trials.

What are some common challenges faced by professionals working in IBM Clinical Development, and how can they be addressed?

Professionals in IBM Clinical Development often encounter challenges such as managing complex clinical trial data, ensuring regulatory compliance, and integrating diverse datasets from multiple sources. These challenges can be addressed by staying current with platform updates, leveraging IBM's training resources, and collaborating closely with cross-functional teams including data managers, clinical researchers, and IT specialists. Proactively communicating with stakeholders and adopting a problem-solving mindset are also key to efficiently navigating project complexities and delivering high-quality outcomes.

What are the key skills and qualifications needed to thrive as an IBM Clinical Development Specialist, and why are they important?

To thrive as an IBM Clinical Development Specialist, you need a background in life sciences, clinical research, or healthcare, often complemented by a relevant degree or clinical trial certification. Proficiency with IBM Clinical Development (ICD) software, electronic data capture (EDC) systems, and familiarity with regulatory standards like GCP are essential. Strong problem-solving, project management, and communication skills help facilitate collaboration between sponsors, sites, and technology teams. These skills ensure efficient clinical trial management, regulatory compliance, and high-quality data collection for successful study outcomes.

What is the difference between Ibm Clinical Development vs Clinical Research Associate?

AspectIbm Clinical DevelopmentClinical Research Associate
CredentialsBachelor's degree in life sciences or related field; certifications like CCRP are commonBachelor's degree in life sciences; often requires GCP training and certifications
Work EnvironmentPharmaceutical or biotech company, clinical trial teams, office-basedMonitoring clinical sites, on-site visits, office and site work
Industry UsageUsed within pharmaceutical companies, biotech firms, and clinical trial organizationsCommonly employed in clinical research organizations and pharmaceutical companies

While both roles involve clinical trials, Ibm Clinical Development typically refers to roles within the development phase of clinical products, focusing on data management and protocol adherence. Clinical Research Associates primarily monitor and oversee clinical trial sites to ensure compliance. Both roles require similar educational backgrounds and certifications, but their daily responsibilities and work environments differ slightly.

Is IBM a good entry level job?

An IBM Clinical Development role can be suitable for entry-level candidates interested in clinical research and healthcare technology. These positions often require basic knowledge of clinical trial processes and may offer training, making them accessible to recent graduates or those new to the industry.
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Ibm Clinical Development jobs near you
Manager, Clinical Data Management

Manager, Clinical Data Management

Axsome Therapeutics

New York, NY • On-site

Full-time

Posted 13 days ago

Job description

Axsome Therapeutics is a biopharmaceutical company leading a new era in the treatment of central nervous system (CNS) conditions. We deliver scientific breakthroughs by identifying critical gaps in care and develop differentiated products with a focus on novel mechanisms of action that enable meaningful advancements in patient outcomes. Our industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, and multiple late-stage development programs addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Together, we are on a mission to solve some of the brain's biggest problems so patients and their loved ones can flourish. For more information, please visit us at www.axsome.com and follow us on LinkedIn and X.
About This Role
Axsome Therapeutics is seeking a Manager, Data Management to be responsible for conducting and overseeing all data management aspects for assigned clinical program(s) in compliance with ICH GCP, regulatory guidelines/standards and applicable SOPs. Tasks include collaborating cross-functionally with study teams, providing DM expertise and conducting all data management activities, overseeing vendors, timelines, costs, resources, and key project deliverables.
This role is based at Axsome's HQ in New York City with an on-site requirement of at least three days per week. We are unable to consider candidates who are looking for fully remote roles.
Job Responsibilities and Duties include, but are not limited to, the following:
  • Data management oversight of multiple clinical development programs in addition to serving as the lead clinical data manager on designated programs as needed
  • Responsible for data related vendor selection and oversight activities across multiple clinical development programs
  • Oversee the planning and management of Data Management costs and timelines
  • Represent data management function on the clinical and cross-functional team meetings ensuring aligned expectations between all parties, including outside vendors.
  • Ensure achievement of major data management deliverables and milestones in coordination with other functions including Clinical Operations, Safety, Statistics, etc.
  • Responsible for drafting safety and other customized data listings/metrics/reports to drive activities such as medical reviews, clinical reviews and risk-based monitoring
  • Participate and represent data management function in during audits and inspections as requested.
  • Author, review, and revise Standard Operating Procedures (SOPs)
  • Draft/review Data Management Plans, data entry guidelines, data management reports and other documents
  • Lead the development and user acceptance testing of Case Report Forms (CRFs) and edit check specifications per protocol, across the lifecycle of the study
  • Manage external data transfers, reconciliations, and system integrations
  • Lead the process of cleaning databases by performing a review of clinical trial data through EDC or data listings
  • Generate queries to appropriate internal or external personnel (e.g. - investigational sites, vendors, Clinical Research Associates) to resolve problematic data identified during every aspect of the data management process
  • Review responses to queries for appropriateness and resolution to ensure high data quality
  • Train team members on Axsome procedures, study specific handling and management of Data Management systems
  • May also act to supervise and mentor data management staff
  • Ensure archival of all Data Management Trial Master File (TMF) documents

Requirements / Qualifications
  • Bachelor's degree required. Preference to candidates with a scientific background (RN, MS, MD, PharmD, PhD or similar)
  • Minimum of 4 - 7 years data management experience in a biotech/pharmaceutical company or clinical research organization (CRO)
  • Thorough understanding of FDA, GCP and ICH guidelines
  • Strong knowledge of EDC and/or systems design (i.e., Merative Zelta (IBM Clinical), Veeva, Medrio, Rave, etc.), IRT/IWRS and data warehouse technologies as applied to clinical trials
  • Strong working knowledge of (e)CRF design and data management functions/activities as applied to standards library development and maintenance
  • Good working knowledge of CDISC standards and experience implementing standards preferred
  • Advanced knowledge of Excel
  • Good working knowledge of general statistical programming processes and practices. Advanced knowledge of medical terminology, medical coding, laboratory reference ranges, and clinical procedures
  • Ability to work on site Monday, Tuesday & Thursday. We are unable to consider candidates who are looking for fully remote roles

Experience, Knowledge and Skills
  • Exhibits initiative, strong problem solving and leadership skills
  • Ability to handle multiple programs simultaneously with strong project management capabilities
  • Comfortable multi-tasking in a fast-paced small company environment and able to adjust workload based upon changing priorities
  • Excellent team player: willingness and ability to fill functional gaps in a small but growing organization
  • Preference to energetic candidates with a desire to think "outside the box"
  • Strong attention to detail and excellent organization skills
  • Strong interpersonal skills and communication skills (both written and oral)
  • Embody a culture of continual improvement and innovation; promote knowledge sharing

Salary & Benefits
The anticipated salary range for this role is $125,000 - $140,000. We encourage candidates of all levels to apply as there may be flexibility on final job title and responsibilities. The salary offer will be based on a variety of factors, including experience, qualifications, internal equity and location. Axsome offers a competitive employment package that includes an annual bonus, significant equity and a generous benefits package.
Axsome is committed to equal employment opportunity and providing reasonable accommodations to applicants with physical and/or mental disabilities. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, gender, sex, age, religion, creed, national origin, sexual orientation, gender identity, ancestry, citizenship, marital status, physical or mental disability, medical condition, veteran status, genetic information, or any other characteristic protected by federal, state, or local law.
Axsome Therapeutics does not accept unsolicited resumes from recruiters or third-party recruitment agencies and will not pay placement fees for unsolicited candidates that are sent to hiring managers, the HR team or other Axsome team members. Only approved vendors who have been explicitly asked to support a specific search will receive access to our Applicant Tracking System to submit candidates for consideration.

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