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Wipro Clinical Data Management Jobs (NOW HIRING)

Systimmune

Director, Clinical Data Management

Redmond, WA · On-site

$190K - $250K/yr

SystImmune is seeking an experienced and strategic Director, Clinical Data Management to lead the clinical data management function across our portfolio. This individual will be responsible for ...

Xencor

Director, Clinical Data Management

San Diego, CA · On-site

We have an excellent opportunity for a Director, Clinical Data Management , to join our team. This position will be based out of our San Diego, CA. office and is a minimum 2 days a week onsite hybrid ...

Exelixis

Clinical Data Management Director

Alameda, CA · On-site

The Clinical Data Management (CDM) Director is a highly experienced and influential leader with expert knowledge of Clinical Data Management concepts and processes. This position is accountable for ...

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Wipro Clinical Data Management information

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How much do wipro clinical data management jobs pay per hour?

As of Jul 29, 2026, the average hourly pay for wipro clinical data management in the United States is $57.17, according to ZipRecruiter salary data. Most workers in this role earn between $45.19 and $68.03 per hour, depending on experience, location, and employer.

What is the job role of clinical data management?

Clinical data management involves collecting, cleaning, and maintaining clinical trial data to ensure accuracy, completeness, and consistency. Professionals in this field use specialized software and follow regulatory standards to support data integrity throughout the clinical research process.

What is Wipro Clinical Data Management?

Wipro Clinical Data Management refers to the services and solutions provided by Wipro, a global IT and consulting company, to manage and process clinical trial data for pharmaceutical, biotech, and medical device companies. Their clinical data management services ensure that data collected during clinical trials is accurate, reliable, and compliant with regulatory standards. This involves activities like data entry, validation, cleaning, and maintaining data integrity throughout the trial lifecycle. Wipro utilizes advanced technologies and domain expertise to streamline data management processes, reduce errors, and accelerate drug development timelines.

How much do clinical data managers make?

Clinical data managers in the US typically earn between $70,000 and $110,000 annually, depending on experience, education, and location. Entry-level roles may start around $60,000, while experienced professionals with certifications can earn over $120,000. The role often requires proficiency in data management tools like EDC systems and knowledge of regulatory standards such as GCP and FDA guidelines.

How do I get into clinical data management?

To enter clinical data management, candidates typically need a bachelor's degree in life sciences, healthcare, or related fields. Gaining experience with clinical trial processes, data management tools like EDC systems, and understanding regulatory requirements such as GCP can improve job prospects; certifications like CDMP may also be beneficial.

What are the key skills and qualifications needed to thrive as a Wipro Clinical Data Management professional, and why are they important?

To thrive in Wipro Clinical Data Management, you need a background in life sciences or pharmacy, strong analytical abilities, and knowledge of clinical trial processes. Familiarity with clinical data management systems (like Medidata Rave or Oracle Clinical), Good Clinical Practice (GCP) guidelines, and relevant certifications such as CDM or SAS are highly valuable. Exceptional attention to detail, problem-solving, and effective communication help ensure data integrity and support collaboration across teams. These skills and qualifications are crucial to maintain high-quality clinical data, regulatory compliance, and successful trial outcomes.

What is the difference between Wipro Clinical Data Management vs Wipro Clinical Data Management?

AspectWipro Clinical Data Management

Since the question compares the same job title, Wipro Clinical Data Management, there is no difference between the roles. Both involve managing clinical trial data, ensuring data accuracy, and supporting regulatory submissions within the pharmaceutical and biotech industries. The responsibilities, required skills, and work environment are consistent across positions with this title at Wipro.

What is the salary of data analyst in Wipro?

The salary of a data analyst at Wipro typically ranges from ₹3.5 lakh to ₹8 lakh per year, depending on experience, skills, and location. Entry-level positions may start lower, while experienced analysts with certifications in data tools like SQL or Python can earn higher salaries.

What are some common challenges faced by Clinical Data Management professionals at Wipro, and how can they be addressed?

Clinical Data Management professionals at Wipro often encounter challenges such as managing large volumes of complex clinical trial data, ensuring data quality and compliance with regulatory standards, and coordinating across global teams. These challenges are typically addressed through robust data validation processes, continuous training on regulatory requirements like GCP and ICH guidelines, and effective communication tools for cross-functional collaboration. Wipro supports its teams with advanced data management systems and regular process audits to help maintain high data integrity and streamline workflow.
More about Wipro Clinical Data Management jobs
What states have the most Wipro Clinical Data Management jobs? States with the most job openings for Wipro Clinical Data Management jobs include:
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Wipro Clinical Data Management jobs near you
Infographic showing various Wipro Clinical Data Management job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $118,909 per year, or $57.2 per hour.
Director, Clinical Data Management

Director, Clinical Data Management

SystImmune, Inc

Redmond, WA • On-site

$190K - $250K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 14 days ago

Job description

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
SystImmune is seeking an experienced and strategic Director, Clinical Data Management to lead the clinical data management function across our portfolio. This individual will be responsible for overseeing all aspects of clinical data management activities from study start-up through database lock and regulatory submission. The Director will provide leadership for internal and external data management teams, ensure high-quality and inspection-ready clinical data, and contribute to the development and execution of data management strategies supporting global clinical trials.
The successful candidate will collaborate closely with Clinical Operations, Biostatistics, Statistical Programming, Clinical Development, Pharmacovigilance, Regulatory Affairs, and external partners to ensure timely and compliant delivery of clinical data for decision-making and regulatory submissions.
This position is full-time onsite and can work out of our Redmond, WA or Princeton, NJ locations.
Responsibilities
  • Lead and oversee the Clinical Data Management function, including strategy, standards, processes, and operational execution across the development portfolio.
  • Build and scale a high-performing data management infrastructure to support a growing clinical pipeline.
  • Serve as a key cross-functional leader in clinical development planning and execution.
  • Oversee all data management activities for Phase I-III clinical trials from study start-up through database lock and regulatory submission.
  • Ensure the delivery of high-quality, complete, and reliable clinical data through effective data review, issue management, and quality oversight.
  • Drive timely database lock and submission-ready data deliverables in accordance with study timelines.
  • Ensure compliance with ICH-GCP, FDA, EMA, and other applicable regulatory requirements, while maintaining inspection readiness.
  • Establish and maintain CDISC-compliant data standards and industry best practices to support regulatory submissions.
  • Collaborate closely with Clinical Operations, Biostatistics, Statistical Programming, Medical Monitoring, and Safety teams to support study execution, data review, and submission readiness.

Qualifications
  • Bachelor's degree in Life Sciences, Computer Science, Statistics, or a related field required; Master's degree preferred.
  • Minimum 10 years of clinical data management experience within the pharmaceutical, biotechnology, or CRO industry.
  • At least 5 years of leadership experience managing data management teams, vendors, and CRO partnerships.
  • Significant experience supporting oncology clinical trials across early- and late-stage development.
  • Demonstrated experience supporting regulatory submissions (NDA, BLA, MAA) and health authority inspections.
  • Expertise with EDC systems, external data integrations, data reconciliation, and database management.
  • Strong knowledge of clinical trial databases, CDISC standards, coding dictionaries (e.g., MedDRA, WHO Drug), and clinical data workflows.
  • Familiarity with risk-based quality management principles, GCP requirements, and clinical development processes.
  • Working knowledge of biostatistics, statistical analysis, and clinical data reporting to support cross-functional collaboration.
  • Proven leadership, strategic thinking, problem-solving, communication, and stakeholder management skills, with a track record of driving cross-functional collaboration and operational excellence in a fast-paced biotech environment.

Preferred Qualifications
  • Oncology and/or antibody-drug conjugate (ADC) development experience.
  • Experience managing global clinical trials across multiple regions.
  • Prior experience in a growing biotechnology company.

Compensation and Benefits:
The expected base salary range for this position is $190,000 - $250,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate's level qualifications, experience, and skills.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company's success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.

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