Clinical Research Physician ( {{city}}) Job at Medix, Watertown, MA

eTJPOGRQcTVxR1pDaTFwYjJ3UU9oNmlpQXc9PQ==
  • Medix
  • Watertown, MA

Job Description

We are currently searching for an experienced physician to work full time (Mon - Fri) Onsite in Watertown MA as a sub Investigator on our industry sponsored clinical research trials. We are open to a variety of backgrounds including: Sleep Disorders, Psychiatry, Neurology, Anesthesiology, Emergency Medicine, and Internal Medicine.

The ideal candidate will also be able to read EKG's.

Previous clinical research experience is not required.

Sub Investigators play a crucial role in supporting the Principal Investigator (PI) to ensure the study is conducted according to the protocol, Good Clinical Practice (GCP), and regulatory requirements. Below are the standard responsibilities of a Sub-Investigator:

🔹 Clinical Oversight

  • Conduct study-related procedures delegated by the PI (e.g., physical exams, medical assessments, reviewing labs).
  • Ensure participant safety and evaluate adverse events.
  • Assist in determining participant eligibility and informed consent process.

🔹 Protocol Adherence

  • Understand and follow the study protocol and amendments.
  • Report protocol deviations promptly to the PI and study sponsor.

🔹 Documentation & Data Integrity

  • Accurately complete source documents and case report forms (CRFs).
  • Review and verify data entered into the electronic data capture (EDC) system.
  • Maintain accurate and timely medical records.

🔹 Regulatory & Compliance

  • Comply with ICH-GCP guidelines, FDA regulations, and institutional SOPs.
  • Participate in site monitoring visits, audits, and inspections as needed.
  • Report adverse events (AEs) and serious adverse events (SAEs) in accordance with regulatory timelines.

🔹 Patient Interaction

  • Provide direct clinical care to study participants.
  • Educate participants about the study, investigational product, procedures, and potential risks/benefits.
  • Ensure participants rights, safety, and well-being are protected throughout the study.

🔹 Collaboration with Study Team

  • Work closely with the PI, study coordinators, and sponsor representatives.
  • Attend investigator meetings, site initiation visits, and protocol training sessions when required.

Job Tags

Full time, Part time,

Similar Jobs

Centra Health

PMHNP - Consult-Liaison/Psych Emergency Services Job at Centra Health

 ...Centra Lynchburg General Hospital (358-bed facility) Offer telehealth consults to Virginia Baptist Hospital and other CMG emergency...  ...hires Strong administrative support Requirements M.S. in Nursing required Psychiatry and Mental Health Nurse Practitioner (... 

Labcorp

Phlebotomist Job at Labcorp

 ...Phlebotomist at Labcorp summary: A Phlebotomist at Labcorp performs blood specimen collections using venipuncture and capillary techniques...  ..., manage specimen and patient information logs, and may travel to additional sites as needed. This role requires certification... 

Extra Multi-Ressources

Chauffeur classe 1 (Roll-Off départ de Amos 28$/h) Job at Extra Multi-Ressources

 ...Ce que nous recherchons: Classe1 Mention FM Exprience minimum de 2ans Dossier de conduite impeccable Exprience en Roll-Off un atout Vous devez aussi avoir votre passeport valide car occasionnellement vous aller dcharger ou charger prs des lignes amricaines... 

Bloomsbury Academy

Teacher Assistant (ECA) Job at Bloomsbury Academy

About the Role: As the Early Childhood Assistant, you will work under the direction of the Supervisor and report to the Director/Supervisor of Bloomsbury Academy. You will assist in planning and developing age-appropriate programs to enhance the cognitive, physical, social...

Pizza Hut

restaurant assistant manager Job at Pizza Hut

Overview Languages English Education ~ College, CEGEP or other non-university certificate or diploma from a program of 1 year to 2 years Experience Experience an asset On site Work must be completed at the physical location. There is no option...