Milestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP, protocol requirements within Study specific defined timelines and enrollment goals.
Responsibilities
Act as the main line of communication between the Sponsor or CRO and the site
Ensure response to feasibility questions are provided in due time
Assist in scheduling and preparation for all types of monitoring visits at the medical institution/research center
Be present and available to respond to monitors during all types of monitoring visits conducted at the medical institution
Track patient enrollment and actively support the medical site and CRO/Sponsor team in meeting project timelines and enrollment goals
Requirements
College or university degree in Life Science, preferably in pharmacy, nursing or lab analytics
Serve as a key team member within the clinical research site, overseeing complex studies while supporting staff development, operational performance, and high-quality patient experiences.
Responsibilities
Lead and independently manage complex industry-sponsored clinical trials from study start-up through closeout
Coordinate complex study visit schedules and protocol-related activities while ensuring compliance with study timelines and regulatory requirements
Lead patient recruitment and retention initiatives to support enrollment performance and patient engagement goals
Mentor and support junior coordinators and research staff on clinical trial processes, patient interactions, sponsor communication, and operational best practices
Conduct protocol-required patient visits and assessments in accordance with study protocols, GCP guidelines, and site SOPs
Requirements
Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline
Principal Database Programmer (eCOA Study Builder / Designer) specializing in electronic Clinical Outcome Assessment (eCOA) solutions to join our team in a Remote/Hybrid/On-site(Hyderabad or Bengaluru) capacity. You will provide technical expertise for the design, configuration, testing, deployment, and maintenance of eCOA solutions used in clinical trials.
Locations (2)
Hyderabad, Telangana, India
Bengaluru, Karnataka, India
Responsibilities
Design, set up, maintain, revise, and close out eCOA studies by interpreting protocols, schedules of assessments, eCOA specifications, and licensed instrument requirements
Configure questionnaires, screens, field properties, code lists, schedules, branching logic, rules, reminders, alerts, notifications, and study settings in the approved eCOA platform
Coordinate the initial eCOA configuration and controlled push to EDC, maintaining alignment among the eCOA configuration, EDC draft, and applicable CRF versions
Assess and implement approved protocol amendments, production revisions, translations, and study maintenance changes while protecting data integrity and traceability
The Clinical Research Coordinator (CRC) - Intermediate champions patient safety and protocol integrity while upholding the highest standards of patient care, coordinating all on-study activities for clinical trials.
Responsibilities
Screening and scheduling patients
Coordinating all on-study activities
Maintaining compliance with study requirements
Participating in study teleconferences with sponsors and clinical research organizations
Ensuring timely and accurate reporting of serious adverse events, unanticipated problems, deviations, and noncompliance to the IRB and study sponsor
Requirements
Bachelor's degree
Nice to have: Knowledge of Federal regulations and ethical standards governing human subjects research (e.g., FDA, HIPAA, IRB processes)
Nice to have: Basic understanding of Clinical trial design, methodology, and protocol requirements
The Clinical Data Coordinator is responsible for clinical data entry activities for the Caris Medical Affairs protocols and projects at the Caris Precision Oncology Alliance sites. The position will ensure the highest standards for clinical data integrity and quality are maintained in alignment with critical research efforts aimed to improve the treatment, health and medical outcomes for oncology patients.
Responsibilities
Abstract clinical data from subject source documentation
Enter clinical data into the study specific EDC case report forms
Clean the clinical data to verify accuracy
Update the EDC following verification of subject data, including the resolution of data queries
Track site goals and case report form completion
Requirements
High School Diploma or equivalent
Nice to have: Bachelor’s degree
Nice to have: Research Coordinator Certification (SoCRA, ACRP)
Senior Clinical Research Associate (Senior CRA) at Magnus Medical, a medical device company focused on advancing treatments in mental health, responsible for overseeing the execution of clinical trials from site selection through close-out, ensuring adherence to study protocols, regulatory guidelines, and Good Clinical Practice (GCP).
Compensation
Salary Range: $140,000 - $165,000 Annually
The annual base salary range for this position based in the United States is noted. This range is an estimate, and actual salary may vary based on Magnus' compensation practices, job-related skills, depth of experience, relevant certifications and training, and geographic location. Magnus utilizes the full width of the range. Our compensation package also includes an annual bonus based on company goals and an equity grant.
Responsibilities
Independently manage clinical monitoring activities for assigned clinical trial sites including site selection/qualification, initiation, routine monitoring, and close-out visits.
Serve as a key liaison between Magnus and clinical trial sites, building strong site relationships and ensuring high engagement in trials involving sensitive patient populations.
Collaborate effectively with peers and leadership across departments and professionally interact/build relationships with investigators, key opinion leaders etc.
Ensure the accuracy and integrity of data by reviewing source documents and case report forms (CRFs), with attention to detail.
Monitor protocol compliance, subject safety, informed consent processes, and the proper administration of psychiatric scales.
Requirements
Bachelor’s or advanced degree in Life Sciences
Senior Clinical Research Associate -Oncology/CNS (Poland)
Lead site qualification, initiation, monitoring, and close‑out activities for oncology/CNS clinical trials in Poland, ensuring GCP and regulatory compliance.
Responsibilities
Lead site qualification, initiation, interim monitoring, management, and close‑out activities in line with study protocols, GCP, regulatory requirements, and SOPs.
Monitor study quality and patient safety through source document verification, informed consent and safety information review, CRF review, and support with data query resolution.
Build effective relationships with investigators and site teams, providing ongoing communication, protocol guidance, training, and support throughout the study lifecycle.
Ensure essential regulatory, ethics, Investigator Site File, TMF, and investigational product documentation and accountability requirements are appropriately maintained.
Partner with Project Management and study teams to evaluate deliverables, study milestones, site performance, and monitoring requirements.
Requirements
MD or Pharmacy degree with at least 3 years of CRA experience
Four‑year degree in medical, biological, physical, health, pharmacy, or a related science with at least 5 years of CRA experience
Two‑year college curriculum or equivalent education/training, preferably in nursing or life sciences, with at least 7 years of CRA experience
The Director, Clinical Scientist serves as a scientific and clinical development leader responsible for supporting the strategy, design, execution, interpretation, and communication of Dyne’s clinical studies.
Compensation
MA Pay Range
$222,000—$258,000 USD
Responsibilities
Lead clinical development strategy and study leadership
Provide scientific input into study design, patient population, eligibility criteria, endpoints, biomarkers, assessments, visit schedules, and data collection strategies
Interpret emerging clinical data and translate findings into clear recommendations for study conduct, clinical development strategy, internal governance discussions, regulatory interactions, and external scientific communications
Maintain current knowledge of rare disease, neuromuscular disease, genetic medicine, oligonucleotide therapeutics, clinical trial innovation, regulatory expectations, competitive developments, and relevant scientific literature
Partner closely with Clinical Operations, Biostatistics, Data Management, Pharmacovigilance, Regulatory Affairs, Translational Medicine, Medical Affairs, Quality, CROs, vendors, and other stakeholders to support high-quality study execution
Requirements
Advanced degree in life sciences, healthcare, pharmacy, medicine, nursing, or a clinically relevant discipline
PhD
PharmD
MD
Nice to have: rare disease
Research Assistant II
Portland VA Research Foundation · Posted Nov 10, 2026
Oversee and coordinate global clinical trials from initiation through to completion, ensuring compliance, managing timelines, budgets, and stakeholder communication.
Compensation
The expected base salary range for this position is $150,000- $180,000 annually.
Responsibilities
Oversee the planning and execution of global clinical trials
Develop and implement study protocols, timelines, and budgets
Manage all aspects of clinical trial operations, including site selection, initiation, monitoring, and closeout
Ensure compliance with Good Clinical Practice (GCP) and regulatory guidelines
Coordinate with cross-functional teams, including investigators, vendors, and regulatory bodies
Requirements
Bachelor’s degree in Life Sciences, Nursing, or a related field
Master’s degree in a related field or clinical research certification (e.g., ACRP or SOCRA)
Nice to have: experience in managing global oncology trials
Nice to have: experience in a sponsor or CRO environment
Nice to have: Master’s degree or clinical research certification
Senior Clinical Research CoordinatorNewIterative Health · Providence, US
CTO Clinical Research Coordinator - IntermediateNewUT Health San Antonio · San Antonio, US
Senior Clinical Research AssociateMagnus Medical · US
Senior Clinical Research Associate -Oncology/CNS (Poland)Lifelancer · Remote, Poland
Director, Clinical ScientistDyne Therapeutics · Waltham, US
Research Assistant IIPortland VA Research Foundation · Portland, US
Associate Director, Clinical Project Management - OncologySystimmune · Princeton, US