PRO-CTCAE Implementation Manager Candidates Sample Search Report

90%

J* D**

Clinical Data Quality Manager at National Cancer Institute

Bethesda, Maryland, United States

This person is currently working as a Clinical Data Quality Manager for the National Cancer Institute, indicating direct experience with NCI operations and clinical data quality, making them a very strong fit despite the exact title mismatch. Clinical Data Quality Manager at NCI. Strong.

LinkedIn Email Phone

Work Experience

National Cancer Institute

Clinical Data Quality Manager

Qualification Criteria 3 met, 2 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

data quality clinical

90%

S C

Clinical Data Manager at NIH/NCI

Washington, District of Columbia, United States 7 years 10 months

This individual has explicit experience as a Clinical Data Manager at NIH/NCI, making the NCI cooperative groups match very likely, and they manage data throughout the study lifecycle, suggesting relevance to implementation, though PRO-CTCAE itself is unconfirmed. CDM at NIH/NCI, 7+ years experience in oncology data management. Excellent.

LinkedIn Email Phone

Work Experience

Omni Eye Specialists - Maryland

Ophthalmic Technician · 3 years

American Center for Community Integration Services

Case Manager · 1 year

National Institute of Cancer at the National Institutes of Health (ASRC Federal)

Clinical Data Manager · 3 years 10 months

Qualification Criteria 3 met, 1 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

user acceptance testing clinical healthcare oncology database integrity management supervising validation testing gcp compliance +8 more

90%

A B

Senior Manager, Clinical Research Data Management, ASCO

Wesley Chapel, Florida, United States 15 years 2 months

This individual is a strong fit, working in a Senior Manager role at ASCO (closely related to NCI groups) managing clinical research data, indicating relevant functional background even if PRO-CTCAE system details are partial. ASCO, 15 years in Clinical Research Data Management/Project Management. Strong.

LinkedIn Email Phone

Work Experience

University of South Florida’s College of Public Health

CREATE Research Scholar · 9 months

Peace Corps

Monitoring And Evaluation Specialist · 2 years 3 months

M2GEN

Medical Informatics Analyst II · 2 years 8 months

Botswana-UPenn Partnership

Clinical Research Associate · 9 months

+ 6 more positions

Qualification Criteria 3 met

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

management oncology infrastructure budgets clinical research health benefits wellness irb evaluation curating +8 more

85%

V N

Associate Director, Clinical Data Standards at Takeda

Lexington, Massachusetts, United States 27 years 1 month

Direct experience within an NCI cooperative group and data standards management strongly aligns with the specialized nature of this role, though the specific manager title might differ slightly. Team Lead at Harvard Clinical Research Institute → various management/standards roles, including Clinical Programmer at Eastern Cooperative Oncology Group. Strong.

LinkedIn Email Phone

Work Experience

Takeda

Associate Director, Data Standards

Harvard Clinical Research Institute

Team Lead

Tolerx, Inc.

Business Systems Project Manager

Millennium Pharmaceuticals

Consultant

+ 6 more positions

Qualification Criteria 3 met

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

project manager director clinical software

80%

E C

Clinical Data Scientist at Pfizer

Philadelphia, Pennsylvania, United States 16 years 1 month

Strong history in clinical data management, EDC systems design, and quality control, which aligns well with the implementation aspect, although PRO/CTCAE systems are not explicitly named. Clinical Data Scientist/Senior Data Manager at Pfizer → CRC at UPenn. Strong.

LinkedIn Email Phone

Work Experience

Einstein Medical Center Philadelphia

Undergraduate Intern · 2 months

The Children's Hospital of Philadelphia

Undergraduate Intern · 2 months

University of Pennsylvania School of Medicine

Clinical Research Coordinator · 2 years 11 months

Pfizer

Senior Data Manager · 2 years 5 months

+ 6 more positions

Qualification Criteria 2 met, 2 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

clinical reports writing research design collaboration efficiency sop training manuals responsible mentoring +3 more

75%

L* H**

Sr. Clinical Data Management Associate

Philadelphia, Pennsylvania, United States 9 years 3 months

This candidate has significant recent clinical data management experience in complex oncology studies, suggesting exposure to relevant domains, though specific system/group references are missing. Sr. Manager, Cdm at BioNTech SE → Sr. Cdm Assoc at Gilead → Cdm Assoc II at Biosplice → Assoc Project Lead, Cdm at Biosplice. Strong.

LinkedIn Email Phone

Work Experience

BioNTech SE

Sr. Manager, Clinical Data Management

Gilead Sciences

Clinical Data Management Associate II

Biosplice Therapeutics

Clinical Trials Assistant

Biosplice Therapeutics

Clinical Data Analyst I

+ 3 more positions

Qualification Criteria 2 met, 3 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

clinical data management clinical management oncology responsible collaboration cdma trials database maintenance risk reconciliation +8 more

75%

P M

Clinical Data Management Manager at Amgen

Berkeley, California, United States 25 years

This is a very experienced Clinical Data Management leader, suggesting broad clinical trials data collection skills, but the specific focus on PRO-CTCAE or NCI groups is not evident. Clinical Data Management Manager at Amgen for a long tenure, extensive DM strategy and oversight experience. Strong.

LinkedIn Email Phone

Work Experience

Adaptimmune US

Clinical Data Manager, Biometrics Department · 2 years 6 months

Amgen

Clinical Data Management Manager - Global Study Operations

UC Merced

Student Researcher in Cognition & Integrated Action Laboratory, Department of Cog.Sci. · 4 months

Amgen

Data Management Senior Manager

+ 6 more positions

Qualification Criteria 2 met, 3 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

data management results oriented clinical trials acceptance testing data quality continuous improvement quality control quality assurance molecular biology data entry data visualization data acquisition +8 more

75%

F** D*

Clinical Data Reporting and Analytics

Princeton, New Jersey, United States 28 years 3 months

This candidate explicitly maintains clinical data management systems and reports to study groups, covering core data activities, and mentions working in accordance with NNI SOPs, which suggests experience in regulated environments, although specific PRO-CTCAE or NCI mention is absent. Associate Director, Clinical Data Reporting and Analytics → BMS/Otsuka/Novo Nordisk, 28+ years experience. Strong.

LinkedIn Email Phone

Work Experience

PharmaNet/i3 (an inVentiv Health Company)

Principal Clinical Data Management Programmer · 1 year 7 months

PharmaNet

Senior Database Programmer · 1 year 5 months

Advanced Biomedical Research, Inc.

Senior Oracle Clinical Database Administrator · 3 years 4 months

Miami University

Post Doctoral Research Scientist · 3 years 4 months

+ 6 more positions

Qualification Criteria 2 met, 3 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

clinical data management data management oracle clinical database administration data mining data cleaning regulatory requirements data quality performance metrics strategic planning system development business development +8 more

75%

K S

Operations Data Manager at Duke Clinical Research Institute

Buford, Georgia, United States 17 years 1 month

Strong clinical data operations background, including software implementation experience, but specific mention of PRO-CTCAE or NCI groups is missing. Operations Data Manager at Duke CRC → Allergan → Ludwig Inst. for Cancer Research → Medidata. Strong.

LinkedIn Email Phone

Work Experience

Duke Clinical Research Institute

Data Operations Manager · 6 years 7 months

Ludwig Institute for Cancer Research

Lead EDC Developer / Clinical Data Manager · 4 years 3 months

Medidata Solutions

Software Implementation Consultant · 3 years 1 month

Allergan

Project Lead / Sr. Clinical Data Manager · 2 years 4 months

Qualification Criteria 2 met, 3 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

clinical research management software trials operations edc coordination projects design specifications integration +8 more

75%

R K

Sr. Manager - Data Configuration and Validation specialist, Clinical data operations &Standards (CDOS)

Philadelphia, United States 19 years 7 months

Strong focus on data configuration, validation, and integration from EDC/non-EDC sources at major pharma/CRO level, relevant to operationalizing data standards like CTCAE, but PRO-CTCAE is not explicitly mentioned. 19+ years experience, currently Sr Manager at Takeda working on data configuration/validation, previously at ICON/Merck, focusing on standards (CDOS). Strong.

LinkedIn Email Phone

Work Experience

University of Pennsylvania

Clinical Research Assistant · 1 year 11 months

Dr. Reddy's Laboratories

Graduate Intern, Quality Control · 1 year 2 months

GSK

Clinical Data Acquisition & validation Analyst · 5 years

ICON plc

Principal Global Clinical Data Standards Specialist, Client- Merck · 2 years 2 months

+ 3 more positions

Qualification Criteria 2 met, 2 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

clinical validation integrity reliability edc operations preparation analytics safety research governance specifications +8 more

75%

R* M**

Sr. Electronic Data Capture Clinical Research Analyst at City of Hope

La Verne, California, United States 30 years 3 months

Strong clinical research background heavily focused on Oncology and coordinating multi-site studies (like SWOG, which is an NCI group), suggesting relevant context for PRO/CTCAE implementation even if not explicitly named. City of Hope roles, managed SWOG studies. Strong.

LinkedIn Email Phone

Work Experience

City of Hope

DCC Research Project Administrator · 4 years 4 months

City of Hope

Research Study Supervisor · 8 years

City of Hope

Clinical Research Associate · 12 years 7 months

City of Hope

Sr. Electronic Data Capture Clinical Research Analyst · 5 years 6 months

Qualification Criteria 3 met, 1 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

clinical research oncology hematology genetics projects design database irb compliance clinical research quality control +2 more

75%

S S

Schenectady, New York, United States 7 years 10 months

PhD-level leader with extensive data science/management background, including experience at MD Anderson Cancer Center, strongly suggesting exposure to environments dealing with complex clinical data collection common in NCI-affiliated settings, though PRO-CTCAE implementation isn't specified. MD Anderson → Current Director level role. Strong.

LinkedIn Email Phone

Work Experience

Infosys

Data Scientist - Lead Consultant · 1 year 4 months

Bristol-Myers Squibb

Sr. Clinical Data Operations & Stewardship Analyst · 2 years 1 month

Kyowa Kirin, Inc.- U.S.

Associate Director, Clinical Data Management · 2 years 7 months

Kyowa Kirin, Inc.- U.S.

Senior Manager, Clinical Data Management · 2 years 2 months

Qualification Criteria 2 met, 2 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

21 cfr part 11 clinical data management creative problem solving root cause analysis data management data science data governance problem solving critical thinking business intelligence big data bayesian statistics +8 more

75%

C B

Senior Data and Quality Assurance Clinical Research Coordinator in Oncology

Pittsburgh, Pennsylvania, United States 15 years 11 months

This specialist has explicit experience working with Children's Oncology Group data entry and quality assurance, making them a strong fit for the cooperative group and clinical data collection aspects, although the title alignment is Coordinator vs Manager. Children's Hospital of Pittsburgh for 12 years specializing in COG data. Strong.

LinkedIn Email Phone

Work Experience

Carlow University

Student Assistant at Carlow University Library, Grace Library · 3 years 9 months

Children's Hospital of Pittsburgh

Clinical Research Associate · 12 years 2 months

Qualification Criteria 3 met, 2 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

oncology assurance clinical research data entry quality assurance clinical research

75%

A E

Director, Clinical Data Management

San Francisco, California, United States 23 years 8 months

Director-level Clinical Data Management experience across major pharma/biotech implies the necessary management skillset and clinical trials background, making this a strong managerial candidate despite the lack of specific PRO-CTCAE/NCI mention. Director at Rain Oncology, formerly Sr Study Data Manager at Genentech/Novartis. Strong.

LinkedIn Email Phone

Work Experience

Genentech

Sr Study Data Manager · 13 years 1 month

Exelixis

Associate Director Clinical Data Management · 1 year 4 months

Novartis (formerly Chiron)

Clinical Data Manager · 5 years 5 months

Rain Oncology

Director, Clinical Data Management

Qualification Criteria 2 met, 3 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

director clinical management data management clinical data management

75%

S L

Data Manager at Roswell Park Cancer Institute

Buffalo, New York, United States 17 years 11 months

Strong experience as Data Manager at an NCI-Designated Center (Roswell Park), indicating familiarity with the ecosystem, and direct experience with clinical trial data collection projects. Data Manager at Roswell Park Cancer Institute → Project Coordinator coordinating intervention trials. Strong.

LinkedIn Email Phone

Work Experience

Roswell Park Cancer Institute

Project Coordinator · 3 years 6 months

Roswell Park Cancer Institute

Data Manager · 13 years 10 months

Qualification Criteria 3 met, 2 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

p less clinical research hipaa operations projects trials prevention irb screening recruitment +5 more

75%

A S

Data Sciences Consultant, eCOA, Clinical Dataflow, Project Management, CDISC, SDTM, Veeva, InForm, ICH GCP, Data Standards

Indianapolis, Indiana, United States 27 years 2 months

Extensive 22 years in clinical data management including driving global data strategy and leading data collection system creation to map to SDTM standards; this strategic implementation background is highly relevant, although PRO-CTCAE specific mention is absent. Pfizer → Eli Lilly. Strong.

LinkedIn Email Phone

Work Experience

Pfizer

Clinical Data Science Manager

Eli Lilly and Company

Clinical Data Management Coordinator · 4 years 10 months

Eli Lilly and Company

Clinical Data Management Associate · 4 years 1 month

Eli Lilly and Company

Consultant Clinical Data · 11 years 11 months

+ 2 more positions

Qualification Criteria 2 met, 2 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

data management pharmaceutical industry data science data collection clinical operations clinical trials data entry regulatory requirements clinical data management clinical management science +8 more

75%

J V

Lead Clinical Data Manager | Biotech & Pharma | Sponsor and CRO Environments

Boston, Massachusetts, United States 7 years 10 months

This individual has strong clinical data management experience, including eCOA setup, which is related to PRO capture, but specific PRO-CTCAE or NCI group experience is missing. Ex-BioNTech → current consultant, 7+ years total experience focusing on CDM, EDC design, and eCOA. Strong.

LinkedIn Email Phone

Work Experience

Selfcare Intuition LLC

Consultant · 1 year 1 month

Cambridge Semantics Inc.

Presales Consultant · 1 year 2 months

BioNTech SE

Clinical Data Management Specialist · 3 years 10 months

ECOG-ACRIN Cancer Research Group

Clinical Data Manager and Performance Monitor · 1 year 11 months

Qualification Criteria 2 met, 3 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

clinical trials presales pain rfp rfi documentation engineering software training management defense +8 more

75%

L N**

Manager, Clinical Operations and Systems at Syneos Health (Previously INC Research/inVentiv Health)

Durham, North Carolina, United States 21 years 9 months

Strong clinical operations management background with experience in systems deployment and training, though PRO-CTCAE and NCI groups are missing. Manager, Clinical Operations and Systems → Manager, Clinical Operations, extensive Phases I-IV experience. Strong.

LinkedIn Email Phone

Work Experience

Syneos Health (Previously INC Research/inVentiv Health)

Manager, Clinical Operations and Systems · 6 years 9 months

PAREXEL

Clinical Monitoring Associate (In House Clinical Research Associate) · 3 years 9 months

QuintilesIMS

Clinical Research Associate · 1 year 2 months

FutureSearch Trials

Clinical Research Manager · 2 years 7 months

+ 3 more positions

Qualification Criteria 2 met, 2 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

clinical trials drug development clinical operations clinical monitoring clinical research regulatory compliance quality assurance recruitment advertising human resources quality improvement software implementation clinical +8 more

75%

J* M**

Clinical Systems Management Professional

Hayward, California, United States 22 years 9 months

This candidate has strong experience managing and implementing clinical systems including ePRO/eCOA, directly relevant to PRO-CTCAE systems implementation, and handles overall clinical systems management for trials. IRT Consultant → Senior Clinical System Lead at ICON. Strong experience in ePRO/eCOA implementation. Strong.

LinkedIn Email Phone

Work Experience

Kaiser Permanente

Clinical Research Associate

Genentech

Global IRT Lead

Converge Consulting, LLC

IRT Consultant

Agios Pharmaceuticals

IRT Systems Manager (consultant)

+ 6 more positions

Qualification Criteria 2 met, 1 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

edc ctms management safety clinical design specifications testing completion validation integration adjustments +8 more

75%

P G

Senior Manager, Clinical Data at Flatiron Health

New York City Metropolitan Area, United States 12 years 11 months

Strong experience in a cancer center setting which often interfaces with cooperative groups, but PRO-CTCAE system work isn't specified. Current/recent roles: Analyst/Lead/Senior Manager at Flatiron Health; prior role at Memorial Sloan Kettering Cancer Center focusing on clinical trial registration and oncology data extraction. Strong.

LinkedIn Email Phone

Work Experience

Flatiron Health

Lead Clinical Data Analyst · 1 year 6 months

Flatiron Health

Manager, Clinical Data

Flatiron Health

Senior Manager, Clinical Data

Memorial Sloan Kettering Cancer Center

Protocol Participant Registration Assistant · 1 year 7 months

+ 2 more positions

Qualification Criteria 2 met, 2 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

clinical registration responsible trials research database integrity training less management physicians reports +6 more

75%

S** C*

Director, Clinical Data Management at MEI Pharma

San Diego, California, United States 20 years 6 months

This Director/Consultant has recent, focused experience in oncology Phase 1a/b studies, including hands-on EDC configuration/issue resolution (Rave URL Admin), showing advanced data collection system management relevant to implementation roles. CDM Consultant (2 projects) → Dir, CDM at MEI Pharma → Assoc Dir, CDM at MEI Pharma → Sr Mgr at MEI Pharma. Strong.

LinkedIn Email Phone

Work Experience

MEI Pharma

Director, Clinical Data Management

Arena Pharmaceuticals

Senior Clinical Data Manager · 2 years 8 months

Biosense Webster

Senior Clinical Data Manager · 1 year 6 months

inVentiv Health Clinical

Senior Clinical Data Manager · 1 year

+ 6 more positions

Qualification Criteria 4 met, 1 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

clinical management oncology projects cro liaison compliance edc database readiness troubleshooting director +7 more

75%

M S

Product Adoption Solution Lead, Professional Services

Chicago, Illinois, United States 17 years 11 months

Strong background implementing and managing electronic solutions for clinical data collection and outcomes assessment (COA), aligning well with PRO-CTCAE implementation, but partnership with NCI cooperative groups is not confirmed. Product Adoption Solution Lead at Professional Services (17+ years exp) specializing in eDC tools like Rave. Strong.

LinkedIn Email Phone

Work Experience

DSP Clinical Research

Senior Clinical Data Manager · 2 years

Medidata Solutions

Senior Project Manager · 6 years 2 months

Baxter Healthcare

Project Manager, Clinical Data Management · 4 years

Medidata Solutions

Client Services Director · 4 months

+ 3 more positions

Qualification Criteria 2 met, 1 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

client services data management project management data collection service delivery oracle clinical executive leadership team leadership staff development relationship management vendor management performance management +8 more

75%

N* S**

Data Management

Kansas City, Missouri, United States 27 years 2 months

This candidate has strong clinical trial experience, including dedicated work on NCTN clinical trials which strongly suggests experience with NCI/cooperative group structures, but no direct mention of PRO-CTCAE. KU Cancer Center (Program Manager NCTN) → PRA Health Sciences, 27+ years. Strong.

LinkedIn Email Phone

Work Experience

Regulatory Clinical Consultants, Inc.

Quality Assurance Specialist · 7 years

PRA Health Sciences

Sr. Clinical Data Coorinator · 3 years

University of KS Cancer Center

Sr. Clinical Research Coordinator · 17 years 2 months

The University of Kansas Cancer Center

Program Manager NCTN Clinical Trials · 5 years 3 months

Qualification Criteria 3 met, 2 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

clinical trials assurance research clinical trials quality assurance clinical research

75%

B A

Senior Project Manager at Medidata Solutions

United States 11 years 1 month

Strong clinical trials experience, especially with CDISC standards, but the employer context isn't clearly an NCI group, and PRO-CTCAE specific skills are missing. Jaeb Center → Medidata, focusing on CDISC mapping and eCRF standards. Strong.

LinkedIn Email Phone

Work Experience

Medidata Solutions

Senior Project Manager · 3 years 8 months

Jaeb Center for Health Research

Clinical Data Manager/Epidemiologist · 3 years 1 month

Centers for Disease Control and Prevention

ORISE Fellow · 7 months

CDISC

Statistical Data Expert for the CDISC T1D Pediatrics & Devices and Exercise Standards Committee · 2 years 7 months

+ 3 more positions

Qualification Criteria 2 met, 2 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

user interface design project manager regulatory requirements data collection clinical trials team development application development user interface focus groups clinical database validation +8 more

75%

N**** I*

Senior Clinical Data Manager @ Denovo Biopharma | Clinical Data Management

Bakersfield, California, United States 7 years 10 months

This candidate has direct experience with an NCI cooperative group and clinical data management tasks, but no direct mention of PRO-CTCAE implementation. Denovo Biopharma → Guardant Health Data Consultant → ECOG-ACRIN (NCI Group) Data Associate. Strong.

LinkedIn Email Phone

Work Experience

Denovo Biopharma

Senior Clinical Data Manager

SDC (Statistics & Data Corporation)

Sr. Clinical Data Associate · 6 months

SDC (Statistics & Data Corporation)

Clinical Data Analyst · 2 years 4 months

Guardant Health

Data Management Consultant

+ 3 more positions

Qualification Criteria 3 met, 2 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

clinical management trials reports specifications operations clinical data management data management data cleaning clinical operations

75%

A* M**

Clinical Research Leader

Charlotte, North Carolina, United States 25 years 8 months

Strong background in clinical trials leadership, including roles at Duke Clinical Research Institute, indicating close proximity to cooperative group work, though PRO-CTCAE specifics are missing. UC San Diego Health Director DM → Duke CRi Project Leader, 25+ years. Strong.

LinkedIn Email Phone

Work Experience

Duke Clinical Research Institute

Clinical Trials Project Leader I · 1 year 11 months

Duke University Health System

Computer Programmer III · 1 year 7 months

Duke University Health System

Computer Project Manager · 2 years 3 months

Duke Clinical Research Institute

Clinical Trials Project Leader II · 3 years 2 months

+ 6 more positions

Qualification Criteria 2 met, 2 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

data management clinical trials project manager systems analysis director management informatics cooperative clinical trials analysis fisma +2 more

75%

B**** L*

Data Manager-Clinical Research Coordinator at University of California, San Francisco

San Francisco, California, United States 6 years 1 month

This candidate mentions direct experience with Cooperative Group Trials, hitting one key requirement, alongside solid data management/CRC work. Data Manager-CRC at UCSF, 6 years total experience. Strong.

LinkedIn Email Phone

Work Experience

University of California, San Francisco

Data Manager-Clinical Research Coordinator · 4 years

University of California, San Francisco

Assistance Clinical Research Coordinator · 1 year 1 month

Qualification Criteria 3 met, 2 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

clinical research maintenance database integrity compliance preparation oncology audit safety cooperative trials +4 more

75%

M V

Clinical Data Specialist III at Duke Clinical Research Institute

United States 17 years 10 months

This candidate currently works at Duke Clinical Research Institute (DCRI), a major NCI affiliate, and has deep data management experience including EDC systems and oncology, making them a potentially strong fit despite lacking the literal job title. Clinical Data Specialist III (DCRI) → extensive CRO/Pharma DM roles, Oncology experience, many EDC systems. Strong.

LinkedIn Email Phone

Work Experience

eClinical Solutions

Senior Clinical Data Manager · 10 months

Tech Observer

Clinical Data Manager (Contract) · 3 years 11 months

PAREXEL

Clinical Data Associate II (Contract) · 5 months

Tech Observer

Clinical Research Associate · 11 months

+ 4 more positions

Qualification Criteria 3 met, 2 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

clinical data management user acceptance testing end user training subject matter experts clinical management cro sop writing designing database testing +8 more

75%

P S

Lead Data Manager at PRA Health Sciences - 20+ years clinical research experience

Quakertown, Pennsylvania, United States 25 years 9 months

This individual has direct experience creating review groups and developing processes for efficacy review of clinical data (similar to PRO data capture/review) within a large clinical research setting (BMS/PRA), indicating high relevance for implementation, though NCI/PRO-CTCAE are absent. Lead Data Manager at PRA Health Sciences → 25+ years experience, primary contact for Review Group (RRG), oversaw efficacy review processes, developed RRG Operations Manual, input into DMP/Edit Check plans. Strong.

LinkedIn Email Phone

Work Experience

PPD

Associate Clinical Data Team Lead II

PRA Health Sciences

Central Review Manager

Quality Data Services, Inc.

Clinical Data Coordinator · 2 years 11 months

SmithKline Beecham Corporation

Clinical Data Coordinator - Contract · 1 year 6 months

+ 5 more positions

Qualification Criteria 2 met, 2 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

risk mitigation data management project management data cleaning acceptance testing project managers quality control quality assurance problem solving user acceptance testing rheumatology physicians +8 more

70%

J* S**

Director, Clinical Data Management at Syneos Health

United States 37 years 10 months

Veteran Director in Clinical Data Management suggests extensive clinical trials experience, but the listed roles heavily feature business engagement and IVRS management, diluting the direct relevance to PRO-CTCAE implementation. Long tenure in CDM/Operations at Covance/Syneos Health. Strong.

LinkedIn Email Phone

Work Experience

Syneos Health

Director, Clinical Data Management

Covance

IVRS Help Desk Manager · 6 years 8 months

Covance

Admin Assistant - Business Development · 1 year

Covance

Project Assistant IVRS · 1 year

+ 6 more positions

Qualification Criteria 2 met, 3 not

PRO-CTCAE systems

NCI cooperative groups

Clinical data collection

Clinical trials experience

PRO-CTCAE Implementation Manager

Skills & Expertise

director clinical management engagement operations training clinical data management data management business development regulatory affairs clinical operations

Candidate Profiles

J*** D****

Work Experience

Qualification Criteria 3 met, 2 not

Skills & Expertise

S**** C****

Work Experience

Qualification Criteria 3 met, 1 not

Skills & Expertise

A**** B****

Work Experience

Qualification Criteria 3 met

Skills & Expertise

V**** N****

Work Experience

Qualification Criteria 3 met

Skills & Expertise

E**** C****

Work Experience

Qualification Criteria 2 met, 2 not

Skills & Expertise

L*** H****

Work Experience

Qualification Criteria 2 met, 3 not

Skills & Expertise

P**** M****

Work Experience

Qualification Criteria 2 met, 3 not

Skills & Expertise

F**** D***

Work Experience

Qualification Criteria 2 met, 3 not

Skills & Expertise

K**** S****

Work Experience

Qualification Criteria 2 met, 3 not

Skills & Expertise

R**** K****

Work Experience

Qualification Criteria 2 met, 2 not

Skills & Expertise

R*** M****

Work Experience

Qualification Criteria 3 met, 1 not

Skills & Expertise

S**** S****

Work Experience

Qualification Criteria 2 met, 2 not

Skills & Expertise

C**** B****

Work Experience

Qualification Criteria 3 met, 2 not

Skills & Expertise

A**** E****

Work Experience

Qualification Criteria 2 met, 3 not

Skills & Expertise

S**** L****

Work Experience

Qualification Criteria 3 met, 2 not

Skills & Expertise

A**** S****

Work Experience

Qualification Criteria 2 met, 2 not

Skills & Expertise

J**** V****

Work Experience

Qualification Criteria 2 met, 3 not

Skills & Expertise

L** N****

Work Experience

Qualification Criteria 2 met, 2 not

Skills & Expertise

J*** M****

Work Experience

Qualification Criteria 2 met, 1 not

Skills & Expertise

P**** G****

Work Experience

Qualification Criteria 2 met, 2 not

J* D**

S C

A B

V N

E C

L* H**

P M

F** D*

K S

R K

R* M**

S S

C B

A E

S L

A S

J V

L N**

J* M**

P G

S** C*

M S

N* S**

B A

A* M**

M V

P S

J* S**