Claims Investigator jobs in Atlantic City, NJ

About Us:

Each of CenExel’s research sites specializes in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well-respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early-phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.

Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.

Job Summary:

On-site physician is responsible for personally supervising or conducting studies according to protocol. Additional responsibilities may include assisting with protocol development and reports, meeting with sponsors and CROs, attending all meetings related to studies, and representing our site as an expert in the field of clinical research.

Essential Responsibilities and Duties:

• Oversees the conduct of research in accordance with federal regulations.

• Assures medical safety and appropriate clinical care for research study participants.

• Supervise research staff.

• Oversees the research team to help ensure ethical conduct in all aspects of the research process including but not limited to the treatment of humans, conflicts of interest, data acquisition, management, sharing and ownership, publication practices, responsible authorship, and collaborative research and reporting.

• Knowledge regarding ongoing and current research studies, research indications, and investigational compounds, with emphasis on patient safety, data collection and protocol execution.

• Attends sponsor training meetings.

• Collection of study data, especially efficacy and safety data-SIGNATURE OVERSIGHT AND INVOLVEMENT.

• Communicates appropriately with entities involved in conducting the research study (eg. Sponsor, CRO, regulatory, vendors, etc).

• Personally responsible for all aspects of training and performance of clinical research staff in executing their responsibilities and duties.

• Documents appropriately assessments, activities, and decisions regarding above responsibilities.

• Maintains records and makes these available for sponsor monitoring, auditing and government inspection.

• On-call coverage.

• Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:

• Possess a valid M.D. or D.O. in Internal Medicine degree. Board Certified or Eligible.

• 1-3 years experience conducting clinical research trials as either a PI or Sub-investigator or other relevant experience.

• Must have good interpersonal skills, demonstrated through interactions with patients, staff, Sponsor representatives, etc.

• Must reflect the professional image of the company, upholding the company vision in actions, demeanor, and appearance. Maintains confidentiality.

• Must possess sound clinical judgment and be able to make decisions regarding subject eligibility, adverse event causality and subject care and follow-up.

Working Conditions

1. Indoor, Clinic and Office environment.

2. Essential physical requirements include sitting, typing, standing, walking.

3. Lightly active position, occasional lifting of up to 20 pounds.

4. Reporting to work, as scheduled, is essential.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.