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About TSR:

TSR is a relationship-based, customer-focused IT and technical services staffing company.

For over 40 years TSR, Inc. and its wholly owned subsidiary, TSR Consulting Services, have prospered in the Information Technology staffing business, earning the respect of companies both large and small with well refined candidate screening, timely placement, and a real understanding of the right skill sets required by our clients.

Mission & Vision

We do not believe in building a vision around the company but building a company around our vision, which is simply;

Every employee’s voice matters, their effort is appreciated, and their talent is rewarded.

We challenge each employee daily, to raise the bar on how we treat our consultants and candidates. For far too long in this industry, candidates have been ghosted, lied to, or placed at a client and then forgotten about. Each day our staff works tirelessly at qualifying and placing, top talent with our clients, in a compassionate and caring manner.

Not every candidate is a match for the job, but every candidate and consultant will be treated with respect and professionalism.


Job Description

  • Location: Lawrence Township, NJ
  • Type: Contract
  • Job #69544

Our client, a leading pharmaceutical company, is hiring a Clinical Research Physician on a contract basis.

Work Location

Lawrence Township, NJ


Basic Responsibilities: The Clinical Research Physician manages and supervises the clinical, scientific, administrative, and technical activities required to conceive, and execute clinical studies within the department with emphasis on overall clinical study leadership. This work is carried out at the direction of senior management in line with departmental strategic goals.

The Clinical Research Physician also is responsible for assisting senior management, in establishing and achieving long-term Corporate Strategic goals and tactical objectives.

Specific Duties (Include, But Are Not Limited To):

1. Provides leadership to the clinical study team involved in the execution of clinical studies.

2. Oversees and is responsible for the quality, coordination and timeliness of protocol development.

3. Oversees and is responsible for the quality, coordination, medical accuracy and timeliness of clinical study reports.

4. Assists senior management to oversee quality, coordination and timeliness of clinical sections of INDs, Investigator Brochures, CTAs, ISSs, ISEs, and clinical expert reports.

5. Participates, as required, as a clinical representative on Project Teams.

6. Establishes and maintains working relationship with Study investigators, key opinion leaders, academicians, and Celgene Senior managers and department heads across the corporation.

7. Ensures adherence to GCP/ICH and Celgene SOP standards.

8. Maintains clinical and scientific awareness in area of expertise.

9. Supports clinical operations in site selection, study budget preparation, study execution and addresses clinical/medical issues at study sites.

10. Participates in the organization, coordination and execution, as required, of internal Celgene meetings and external medical/scientific meetings, e.g., Investigator Meetings and clinical/scientific advisory board meetings.

11. Develops and gives oral presentations, as required.

12. Supports data management as required for CRF development, database edit checks development, listings review, query resolution, database clean-up and lock activities.

13. Prepares clinical study timelines and status reports, as required, per Supervisor.

The position requires an individual with: An advanced degree in a relevant field (MD, Ph.D., Pharm.D or equivalent advanced degree, with experience in clinical research and development.

2-5 years clinical drug development process experience preferred. Knowledge of and strict adherence to GCP/ICH guidelines and internal SOPs in Clinical Research and Development.

Excellent managerial and leadership skills or clear potential to develop such skills.

Excellent verbal communication skills to effectively represent Celgene at a corporate level, with internal working groups/project teams and external academic/industrial/regulatory organizations.

Excellent technical writing written skills. Team player, possesses sense of urgency, is mentorable and exhibits potential for mentoring others.

Skills/Knowledge Required: ORGANIZATIONAL/JUDGEMENT: Must have planning skills to schedule activities to meet Clinical Research and Development and project team deadlines.

The position requires problem solving ability, and skills to address medical, clinical study and technical questions in a multi-disciplinary environment.

Must be technically proficient with standard PC software (Word, Excel, PowerPoint, Desktop products like Outlook). Must keep abreast of medical and scientific literature within the relevant therapeutic area that the individual is working in.

Must maintain high ethical standards and integrity at all times. SUPERVISION: DIRECT and INDIRECT: Supervises internal Clinical Research and Development staff as required.

Also interfaces with CROs, academics, and external experts as appropriate. ACCOUNTABITY: This position has responsibility, for the quality, timeliness, and medical/scientific acceptability of protocols, clinical study execution, and medical accuracy and timeliness of clinical study reports.

This position has cross-functional accountability to the clinical study team and project team, as required. This position must ensure GCP/ICH compliance.

CONTACTS: . INTERNAL: Frequent contact with various levels of R&D as well as moderate contact with colleagues in other departments (regulatory, drug safety, project management, toxicology, drug discovery, marketing, finance, business development, etc


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