DUTIES: • Serve as the DM study lead and the primary point of contact for clinical study teams and external partners, (e.g., external data vendors and CROs) for multiple trials within a given TA ...
DUTIES: • Serve as the DM study lead and the primary point of contact for clinical study teams and external partners, (e.g., external data vendors and CROs) for multiple trials within a given TA ...
Job Advert Posting We are currently seeking a Contractor Senior Clinical Research Associate to join ... Performing data review and resolution of queries to maintain high-quality clinical data.
Job Advert Posting We are currently seeking a Contractor Senior Clinical Research Associate to join ... Performing data review and resolution of queries to maintain high-quality clinical data.
... Senior Clinical Research Associate to join our diverse and dynamic team. This will be for a 6 month ... Performing data review and resolution of queries to maintain high-quality clinical data.
... Senior Clinical Research Associate to join our diverse and dynamic team. This will be for a 6 month ... Performing data review and resolution of queries to maintain high-quality clinical data.
Senior CRA
Blue Bell, PA · Remote
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... Performing data review and resolution of queries to maintain high-quality clinical data.
Senior CRA
Blue Bell, PA · Remote
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... Performing data review and resolution of queries to maintain high-quality clinical data.
Lead Clinical Data Manager (Remote)
Philadelphia, PA · Remote
$68.50K - $217.10K/yr
Your previous roles/job titles may include Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager . * Proven success ...
Lead Clinical Data Manager (Remote)
Philadelphia, PA · Remote
$68.50K - $217.10K/yr
Your previous roles/job titles may include Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager . * Proven success ...
Senior CRA
Blue Bell, PA · Remote
As a Clinical Research Associate at ICON , you will play a pivotal role in designing and analyzing ... Performing data review and resolution of queries to maintain high-quality clinical data.
Senior CRA
Blue Bell, PA · Remote
As a Clinical Research Associate at ICON , you will play a pivotal role in designing and analyzing ... Performing data review and resolution of queries to maintain high-quality clinical data.
Lead Clinical Data Manager (Remote)
Philadelphia, PA · Remote
$68.50K - $217.10K/yr
Your previous roles/job titles may include Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager . * Proven success ...
Lead Clinical Data Manager (Remote)
Philadelphia, PA · Remote
$68.50K - $217.10K/yr
Your previous roles/job titles may include Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager . * Proven success ...
Contract Senior CRA
Blue Bell, PA · Remote
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... Performing data review and resolution of queries to maintain high-quality clinical data.
Contract Senior CRA
Blue Bell, PA · Remote
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... Performing data review and resolution of queries to maintain high-quality clinical data.
Senior CRA
Blue Bell, PA · On-site
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... Performing data review and resolution of queries to maintain high-quality clinical data.
Senior CRA
Blue Bell, PA · On-site
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... Performing data review and resolution of queries to maintain high-quality clinical data.
Act as a leader in industry forums, maintaining network of contacts, and influence industry strategic direction and clinical data standards development. * Build and sustain senior stakeholder ...
Act as a leader in industry forums, maintaining network of contacts, and influence industry strategic direction and clinical data standards development. * Build and sustain senior stakeholder ...
Senior Clinical Research Associate
Blue Bell, PA · On-site +1
Senior Clinical Research Associate - Neurovascular - Midwest/Central ICON plc is a world-leading ... in data integrity, patient safety, and overall quality of clinical trials conducted at ...
Senior Clinical Research Associate
Blue Bell, PA · On-site +1
Senior Clinical Research Associate - Neurovascular - Midwest/Central ICON plc is a world-leading ... in data integrity, patient safety, and overall quality of clinical trials conducted at ...
Senior Clinical Research Associate
Blue Bell, PA · On-site +1
Senior Clinical Research Associate - Neurovascular - Midwest/Central ICON plc is a world-leading ... in data integrity, patient safety, and overall quality of clinical trials conducted at ...
Senior Clinical Research Associate
Blue Bell, PA · On-site +1
Senior Clinical Research Associate - Neurovascular - Midwest/Central ICON plc is a world-leading ... in data integrity, patient safety, and overall quality of clinical trials conducted at ...
Act as a leader in industry forums, maintaining network of contacts, and influence industry strategic direction and clinical data standards development. Build and sustain senior stakeholder networks ...
Act as a leader in industry forums, maintaining network of contacts, and influence industry strategic direction and clinical data standards development. Build and sustain senior stakeholder networks ...
Senior CRA
Blue Bell, PA · On-site
As a Clinical Research Associate at ICON , you will play a pivotal role in designing and analyzing ... Performing data review and resolution of queries to maintain high-quality clinical data.
Senior CRA
Blue Bell, PA · On-site
As a Clinical Research Associate at ICON , you will play a pivotal role in designing and analyzing ... Performing data review and resolution of queries to maintain high-quality clinical data.
Senior Programmer, Clinical Data Evaluation
King Of Prussia, PA · Hybrid
$143K - $169K/yr
The Senior Programmer for Data Validation supports cross-functional teams such as Statistics, Data Management and Standards by overseeing and ensuring the quality of clinical data build and ...
Senior Programmer, Clinical Data Evaluation
King Of Prussia, PA · Hybrid
$143K - $169K/yr
The Senior Programmer for Data Validation supports cross-functional teams such as Statistics, Data Management and Standards by overseeing and ensuring the quality of clinical data build and ...
Contract Senior CRA
Blue Bell, PA · On-site
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... Performing data review and resolution of queries to maintain high-quality clinical data.
Contract Senior CRA
Blue Bell, PA · On-site
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... Performing data review and resolution of queries to maintain high-quality clinical data.
Sr Medidata RAVE Programmer
Radnor, PA · On-site
Sr Medidata RAVE Programmer Contract onsite 4 days a week in Radnor, PA Purpose The Sr Medidata ... Participate in clinical study teleconferences and in person meetings to represent data management ...
Sr Medidata RAVE Programmer
Radnor, PA · On-site
Sr Medidata RAVE Programmer Contract onsite 4 days a week in Radnor, PA Purpose The Sr Medidata ... Participate in clinical study teleconferences and in person meetings to represent data management ...
Director, Clinical Sciences, Oncology
Spring House, PA · On-site +1
$76.40K - $104.10K/yr
... / Sr. Clinical Science Group Leader leads matrix interactions among cross-functional members, contributes to the evaluation of scientific opportunities, medical data monitoring, and drives process ...
Director, Clinical Sciences, Oncology
Spring House, PA · On-site +1
$76.40K - $104.10K/yr
... / Sr. Clinical Science Group Leader leads matrix interactions among cross-functional members, contributes to the evaluation of scientific opportunities, medical data monitoring, and drives process ...
Director, Clinical Sciences, Oncology
Spring House, PA · On-site +1
$76.40K - $104.10K/yr
... / Sr. Clinical Science Group Leader leads matrix interactions among cross-functional members, contributes to the evaluation of scientific opportunities, medical data monitoring, and drives process ...
Director, Clinical Sciences, Oncology
Spring House, PA · On-site +1
$76.40K - $104.10K/yr
... / Sr. Clinical Science Group Leader leads matrix interactions among cross-functional members, contributes to the evaluation of scientific opportunities, medical data monitoring, and drives process ...
Sr. Clinical Research Associate
Blue Bell, PA · On-site +1
Collaborating with cross-functional teams to ensure timely and accurate data collection and ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Sr. Clinical Research Associate
Blue Bell, PA · On-site +1
Collaborating with cross-functional teams to ensure timely and accurate data collection and ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Senior Clinical Data Associate information
See Philadelphia, PA salary details
$39.9K - $43K
9% of jobs
$43K - $46.1K
13% of jobs
$48.2K is the 25th percentile. Wages below this are outliers.
$46.1K - $49.2K
4% of jobs
$49.2K - $52.3K
0% of jobs
$52.3K - $55.5K
0% of jobs
$55.5K - $58.6K
13% of jobs
The median wage is $60.6K / yr.
$58.6K - $61.7K
17% of jobs
$61.7K - $64.8K
11% of jobs
$67K is the 75th percentile. Wages above this are outliers.
$64.8K - $67.9K
13% of jobs
$67.9K - $71K
11% of jobs
$71K - $74.2K
11% of jobs
$39.9K
$59.5K
$74.2K
How much do senior clinical data associate jobs pay per year?
As of May 28, 2026, the average yearly pay for senior clinical data associate in Philadelphia, PA is $59,473.00, according to ZipRecruiter salary data. Most workers in this role earn between $46,400.00 and $68,100.00 per year, depending on experience, location, and employer.
What are the key skills and qualifications needed to thrive as a Senior Clinical Data Associate, and why are they important?
To thrive as a Senior Clinical Data Associate, you need expertise in clinical data management, data cleaning, and knowledge of clinical trial processes, supported by a degree in life sciences or a related field. Familiarity with data management systems like Medidata Rave, EDC platforms, and certifications such as CCDM are commonly required. Attention to detail, strong analytical thinking, and effective communication skills help you excel in ensuring data accuracy and collaborating with cross-functional teams. These capabilities are crucial for maintaining data integrity, regulatory compliance, and the overall success of clinical research studies.
What are some common challenges Senior Clinical Data Associates face when managing large clinical trial datasets?
Senior Clinical Data Associates often manage complex datasets from multiple sites, which can lead to challenges such as ensuring data consistency across sources, resolving discrepancies, and maintaining data integrity under tight timelines. Additionally, they must stay up-to-date with evolving regulatory requirements and work closely with cross-functional teams, including biostatisticians, clinical operations, and data managers, to ensure accurate and timely data delivery. Effective communication, attention to detail, and adaptability are essential to overcome these challenges and ensure successful trial outcomes.
What does a Senior Clinical Data Associate do?
A Senior Clinical Data Associate is responsible for managing and ensuring the accuracy, integrity, and quality of data collected during clinical trials. They oversee data collection processes, review case report forms, resolve data discrepancies, and ensure compliance with regulatory standards. In addition to performing data management tasks, Senior Clinical Data Associates often mentor junior staff, contribute to developing data management plans, and collaborate with clinical research teams to ensure successful trial outcomes.
What are the most commonly searched types of Senior Clinical Data jobs in Philadelphia, PA? The most popular types of Senior Clinical Data jobs in Philadelphia, PA are:
What cities near Philadelphia, PA are hiring for Senior Clinical Data Associate jobs? Cities near Philadelphia, PA with the most Senior Clinical Data Associate job openings:
Full-time
This job post has expired today. Applications are no longer accepted.
Job description
DUTIES:
• Serve as the DM study lead and the primary point of contact for clinical study teams and external partners, (e.g., external data vendors and CROs) for multiple trials within a given TA.
• Lead all aspects of all DM activities across all stages of the trial from study start-up through archiving. Accountable for providing comprehensive program level oversight of SDMs to ensure consistency and compliance of program level standards, track milestones/deliverables, escalate and follow to resolution and communicate program level updates to SDMs
• Provide clear verbal or written information and hands-on support to project team members and to CROs related to eCRF and database design, data quality, and reporting of database / data quality status.
• Interact cross-functionally and provide project leadership for SDMs within the program
• Collaborate with data management peers and other cross functional stakeholders to define and develop operational type of reports to assist with data exploration and metrics.
• Perform & document the oversight of CRO data management activities for assigned studies.
• Data Management Plan (includes: Data Review, Reconciliation and Cleaning, Coding, SAE Recon, Local Lab Handling activities for CRF and non-CRF data
• Lead data transfers with CROs and third-party data sources, SAE/AE reconciliation and MedDRA /WHO-DD coding. • Support the transfer, locking, and archiving of study databases. Lead scheduling and time constrains across multiple projects.
• Prepare recommendations for new or improved processes for data management and data flow. • Ensure the eTMF documentation is maintained on a regular basis for assigned studies
• Perform quality review and inspection readiness tasks to meet quarterly Inspection Readiness Review (IRR) compliance
• Own the implementation and execution of procedures for data quality review and data acceptance prior to data analyses and/or database lock.
• Ensure and manage clinical data are processed according to Good Clinical Practices (GCP), Standard Operating Procedures (SOPs) and Data Handling Guidelines
REQUIREMENTS:
• Serve as the DM study lead and the primary point of contact for clinical study teams and external partners, (e.g., external data vendors and CROs) for multiple trials within a given TA.
• Lead all aspects of all DM activities across all stages of the trial from study start-up through archiving. Accountable for providing comprehensive program level oversight of SDMs to ensure consistency and compliance of program level standards, track milestones/deliverables, escalate and follow to resolution and communicate program level updates to SDMs
• Provide clear verbal or written information and hands-on support to project team members and to CROs related to eCRF and database design, data quality, and reporting of database / data quality status.
• Interact cross-functionally and provide project leadership for SDMs within the program
• Collaborate with data management peers and other cross functional stakeholders to define and develop operational type of reports to assist with data exploration and metrics.
• Perform & document the oversight of CRO data management activities for assigned studies.
• Data Management Plan (includes: Data Review, Reconciliation and Cleaning, Coding, SAE Recon, Local Lab Handling activities for CRF and non-CRF data
• Lead data transfers with CROs and third-party data sources, SAE/AE reconciliation and MedDRA /WHO-DD coding. • Support the transfer, locking, and archiving of study databases. Lead scheduling and time constrains across multiple projects.
• Prepare recommendations for new or improved processes for data management and data flow. • Ensure the eTMF documentation is maintained on a regular basis for assigned studies
• Perform quality review and inspection readiness tasks to meet quarterly Inspection Readiness Review (IRR) compliance
• Own the implementation and execution of procedures for data quality review and data acceptance prior to data analyses and/or database lock.
• Ensure and manage clinical data are processed according to Good Clinical Practices (GCP), Standard Operating Procedures (SOPs) and Data Handling Guidelines
REQUIREMENTS:
- Master's degree Health Administration, Pharmacy or related discipline
- 24 months experience
- Must also have experience with at least one of the following areas/technologies also required: ECS, TMF, CCG, UAT, CRF Specification, QC, DTA/DT
About ACL Digital
Sourced by ZipRecruiter
ACL Digital is a global digital technology firm based in San Jose, CA, US, operating within the IT and services industry. The company offers a broad spectrum of services and solutions, including digital transformation, product engineering, industry solutions, and design-led experiences, among others. ACL Digital has its roots established in 1991 with the aim to become a leading-edge innovator in the digital space and has since grown significantly to work with an array of global customers. The company's mission incorporates a commitment to aiding customers to achieve their business goals by adopting and accelerating their digital transformation journeys.
Industry
Technology, communication and media
Company size
1,001 - 5,000 Employees
Headquarters location
San Jose, CA, US
Year founded
1992