Senior Clinical Research Associate- CNS -Psychiatry - East Coast
$97k - $193kWorldwide Clinical Trials
Worldwide Clinical Trials seeks a Senior Clinical Research Associate to manage site activities for neuroscience studies on the East Coast. The role involves overseeing the full clinical study lifecycle, from site identification through closeout, with regular travel to investigative sites.
Responsibilities
- Manage research activities at investigative sites in assigned studies
- Support sites throughout study lifecycle from initiation through closeout
- Conduct study initiation visits and train sites on data collection and safety reporting
- Monitor site compliance with informed consent, safety reporting, and regulatory requirements
- Coordinate start-up activities including document collection and contract negotiations
Requirements
- Bachelor's degree from four-year university or Nursing degree
- 5+ years experience as Clinical Research Associate
- Psychiatry therapeutic area experience
- Full-service monitoring experience preferred
- Proficiency in Microsoft Office, CTMS, and EDC systems
- Strong written and oral communication skills
- East Coast residency with willingness to travel regionally
Compensation: $97,000–$193,000 annually
$125k - $142k
...Fortrea seeks an experienced Senior Clinical Research Associate for ophthalmology monitoring on the East Coast. The role involves comprehensive site management, data integrity oversight, and regulatory compliance for clinical trials, requiring 5+ years of monitoring experience...SeniorNight shift$100k - $112k
...Fortrea seeks a Clinical Research Associate 2 with oncology experience to monitor clinical trial sites on the East Coast. The role involves 8-10 days monthly onsite, combining site management, data integrity oversight, and regulatory compliance across multiple study locations...SuggestedNight shift- ...Worldwide Clinical Trials seeks a Senior Clinical Research Associate to manage research activities at clinical trial sites, primarily in a remote capacity with... ...regulatory compliance, and ongoing site management across CNS and rare disease programs. Responsibilities...SeniorContract workWork at officeRemote workWorldwide
$87.2k - $169.3k
IQVIA Early Clinical Development is hiring for a Senior CRA 1. Ideal candidates will have Phase 1 experience across... ...therapeutics. Seeking candidates located East Coast, US.Job OverviewWe are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a...SeniorFull timePart timeImmediate startWorldwide$87.2k - $169.3k
...IQVIA is seeking a Senior Clinical Research Associate for early-stage clinical development based on the East Coast. The role involves managing clinical trial sites, ensuring protocol compliance, and maintaining data integrity across Phase 1 and other trial phases. Responsibilities...Senior- ...Senior Clinical Research Associate role focused on CNS and oncology studies at a global CRO. The position involves managing site activities across clinical trials, conducting study initiation visits, and ensuring regulatory compliance, primarily working remotely from...SeniorContract workWork at officeRemote work
$90.2k - $175.1k
IQVIA is now hiring for Clinical Research Associates located on the West Coast and East Coast, US to join our growing Early Clinical Development team working exclusively in Phase I.Job OverviewWe are seeking a dedicated Clinical Research Associate (CRA) to join our team...Full timePart timeImmediate startWorldwide$90.2k - $175.1k
Join a Team That’s Advancing Clinical ResearchWe’re looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role, you’ll partner with investigative sites and cross-functional...SeniorFull timePart timeImmediate startWorldwide$90.2k - $175.1k
...IQVIA seeks a Clinical Research Associate to conduct site monitoring visits and ensure protocol compliance across clinical trials. The role involves building site relationships, managing study progress, and collaborating with cross-functional teams to deliver high-quality...Senior- ...Senior Clinical Research Associate for oncology studies at a global CRO. Manages research activities across participating clinical trial sites, from initiation through closeout, with a focus on regulatory compliance and safety reporting. Requires 5+ years CRA experience...SeniorContract workWork at office
$71.9k - $189k
IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in CNS, GLP-1/Obesity/Diabetes (Type II) and/or Cardiovascular clinical trials. Phase 1 experience is a plus!Job OverviewPerform monitoring and site management work to ensure that sites are...Full timePart timeLocal areaImmediate startWorldwide- Job Title: Clinical Research Associate II (CRA II)Job Location: United States - RemoteJob Overview:The Clinical Research Associate II (CRA II) is responsible for monitoring assigned investigational sites throughout the clinical trial lifecycle. The CRA II serves as the...Interim roleWork at officeRemote work
$74.5k - $197.5k
IQVIA is seeking a Clinical Research Associate II with independent on-site monitoring experience to join our team. We are looking for professionals... ...of the following therapeutic areas:Central Nervous System (CNS)CardiovascularObesityMASH/NASHJob OverviewConduct site...Full timePart timeWork at officeImmediate startWorldwide$100k - $115k
...transplantation, nephrology, immunology, infectious diseases and other underserved conditions. Job Description: The Clinical Research Associate (CRA) is a primarily in-house, sponsor-side Clinical Operations role responsible for supporting clinical trial execution...SeniorRemote work$74.5k - $197.5k
...IQVIA seeks a Clinical Research Associate II to conduct on-site monitoring for clinical trials in therapeutic areas including CNS, cardiovascular, obesity, and NASH/MASH. The role involves site management, regulatory compliance, protocol training, and cross-functional...Work at office$100k - $130k
...Fortrea seeks a Senior Clinical Research Associate with 3+ years of clinical monitoring experience and Phase I trial background for their Durham, North Carolina office. The role involves site monitoring, data integrity oversight, protocol adherence verification, and adverse...SeniorWork at officeLocal areaNight shift- ...as a Batch Release Officer for the review and recommended release of documentation for a range of dosage form batches and finished clinical trial packs of Investigational Medicinal Products in accordance with GMP requirements. • Assessment of Quality QMS Records (e.g....Work experience placementWorldwideShift workDay shift
$90.2k - $197.5k
Role Overview: As a Clinical Research Associate, you’ll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will be pivotal in advancing groundbreaking research.Key Responsibilities:Site Visits: Conduct selection, initiation, monitoring...Full timePart timeWork at officeLocal areaImmediate startWorldwide$90.2k - $175.1k
...IQVIA seeks a Clinical Research Associate to lead site monitoring activities and ensure protocol compliance across clinical trials. The role involves partnering with investigative sites and cross-functional teams to execute studies to GCP/ICH standards while managing regulatory...Senior$105 - $118 per hour
...Clinical Research Associate IIOur Phase I team is currently seeking a Clinical Research Associate II with 1+ years of on-site monitoring experience. Ideal candidates would have phase I experience and reside within the U.S.What You Will DoYou will utilize your skills, knowledge...Work at officeLocal areaNight shift- ...Clinical Research MonitorPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.• Perform site monitoring...Local area
$111k - $309.2k
...scientific services spanning clinical trials, real world... ...rigorous research. This research is broad... ...can be applied to PCS CNS research activities. Individuals... ...ResponsibilitiesAs an Associate Principal within the PCS... ...development (both juniors and seniors) to collaborate with...Full timePart timeImmediate startWorldwide- ...Clinical Research Associate (CRA) Assists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements, ICH/GCP Guidelines, company SOPs, and study protocols. Ensures coordination of interim and closeout activities...Contract workInterim role
$74.5k - $197.5k
...Tampa, FL, United States of America Salt Lake City, UT, United States of America Full time R1573716 Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple Therapeutic Areas | Nationwide Opportunities IQVIA is actively...Full timePart timeWork at officeImmediate startWorldwide$74.5k - $197.5k
...IQVIA seeks experienced Clinical Research Associates II and Senior Clinical Research Associates to oversee clinical trial sites across multiple therapeutic areas nationwide. The role involves managing all phases of site monitoring, ensuring protocol compliance, regulatory...Full timeWork at office$105k - $118k
...Fortrea seeks a Clinical Research Associate II with Phase I experience for on-site monitoring in Durham, North Carolina. The role involves managing clinical trial sites, ensuring protocol compliance, monitoring data integrity, and coordinating study activities with 40-...Night shift- ...Optimapharm is a mid-sized, global Contract Research Organisation (CRO) turning science into hope through agile, patient-focused clinical development. We specialise in Phase I-IV... ...expertise: CRA I → CRA II → CRA III → Senior CRA. Here, your dedication is rewarded...Contract workInterim roleRemote workWorldwide
$90.2k - $190k
...Clinical Research Associate position focused on sponsor-dedicated monitoring and site management for clinical trials. Responsible for conducting site visits, managing recruitment, ensuring protocol compliance, and maintaining regulatory documentation across multiple study...Work at office$100k - $112k
...Fortrea seeks a Clinical Research Associate 2 with 2 years of monitoring experience for oncology clinical trials in the Denver area. The role involves site monitoring, data integrity verification, and regulatory compliance across mixed onsite and remote work, with approximately...Local areaRemote workNight shift$79.5k - $158.5k
...Worldwide Clinical Trials seeks a Clinical Research Associate II with 2–3 years of monitoring experience to support oncology trial execution. The role involves conducting site monitoring visits, ensuring protocol compliance and data integrity, and collaborating with cross...Work at officeRemote workWorldwide
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Senior Clinical Research Associate- CNS -Psychiatry - East Coast. Be the first to apply!
- on-site clinical research associate (traveling/remote) Research Triangle Park, NC
- senior Research Triangle Park, NC
- senior performance engineer Research Triangle Park, NC
- senior software engineer remote Research Triangle Park, NC
- senior activities Research Triangle Park, NC
- senior implementation engineer Research Triangle Park, NC
- srs Research Triangle Park, NC
- senior vice president of operations Research Triangle Park, NC
- senior operations technician Research Triangle Park, NC
- clinical research remote Research Triangle Park, NC



